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dbVar

Database of genomic structural variation

nsv917984

Organism: Homo sapiens

Study:nstd75 (ClinGen Prenatal)
Variant Type:copy number variation
Method Type:Oligo aCGH
Submitted on:NCBI36 (hg18)

Variant Calls:2
Validation:Not tested
Clinical Assertions: Yes
Region Size:101,816

Publication(s):Wapner et al. 2012

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 436 SVs from 37 studies. See in: genome view

Remapped(Score: Perfect):8,625,244-8,727,059

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv917984	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	8,625,244	8,727,059
nsv917984	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	8,593,285	8,695,100
nsv917984	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000023.9	ChrX	8,553,285	8,655,100

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	Copy number
nssv1606370	copy number gain	ISCA_ID_pn_2011	Oligo aCGH	Probe signal intensity	Increased nuchal translucency	Benign	Submitter	3
nssv1607577	copy number gain	ISCA_ID_pn_935	Oligo aCGH	Probe signal intensity	Developmental delay AND/OR other significant developmental or morphological phenotypes	Benign	Submitter	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv1606370	Remapped	Perfect	NC_000023.11:g.(?_ 8625244)_(8727059_ ?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	8,625,244	8,727,059
nssv1607577	Remapped	Perfect	NC_000023.11:g.(?_ 8625244)_(8727059_ ?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	8,625,244	8,727,059
nssv1606370	Remapped	Perfect	NC_000023.10:g.(?_ 8593285)_(8695100_ ?)dup	GRCh37.p13	First Pass	NC_000023.10	ChrX	8,593,285	8,695,100
nssv1607577	Remapped	Perfect	NC_000023.10:g.(?_ 8593285)_(8695100_ ?)dup	GRCh37.p13	First Pass	NC_000023.10	ChrX	8,593,285	8,695,100
nssv1606370	Submitted genomic		NC_000023.9:g.(?_8 553285)_(8655100_? )dup	NCBI36 (hg18)		NC_000023.9	ChrX	8,553,285	8,655,100
nssv1607577	Submitted genomic		NC_000023.9:g.(?_8 553285)_(8655100_? )dup	NCBI36 (hg18)		NC_000023.9	ChrX	8,553,285	8,655,100

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	Sample ID	HGVS	Type	Subject Phenotype	Clinical Interpretation	Source of Interpretation	Gender	Age	Copy number
nssv1606370	ISCA_ID_pn_2011	NCBI36: NC_000023.9:g.(?_8553285)_(8655100_?)dup	copy number gain	Increased nuchal translucency	Benign	Submitter	Female	14 weeks gestation	3
nssv1607577	ISCA_ID_pn_935	NCBI36: NC_000023.9:g.(?_8553285)_(8655100_?)dup	copy number gain	Developmental delay AND/OR other significant developmental or morphological phenotypes	Benign	Submitter	Female	12 weeks gestation	3

No genotype data were submitted for this variant

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