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dbVar

Database of genomic structural variation

nsv3892035

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:2,703,111

Description:GRCh37/hg19 20p11.22-11.21(chr20:21680345-24383453)x1 AND See cases

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: 6458 SVs from 100 studies. See in: genome view

Remapped(Score: Perfect):21,699,707-24,402,817

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3892035	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	21,699,707	24,402,817
nsv3892035	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000020.10	Chr20	21,680,345	24,383,453

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15131690	copy number loss	Multiple	Multiple	See cases	Likely pathogenic	ClinVar	RCV000663385.2, VCV000548966.2	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15131690	Remapped	Perfect	NC_000020.11:g.(?_ 21699707)_(2440281 7_?)del	GRCh38.p12	First Pass	NC_000020.11	Chr20	21,699,707	24,402,817
nssv15131690	Submitted genomic		NC_000020.10:g.(?_ 21680345)_(2438345 3_?)del	GRCh37 (hg19)		NC_000020.10	Chr20	21,680,345	24,383,453

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	HGVS	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15131690	GRCh37: NC_000020.10:g.(?_21680345)_(24383453_?)del	copy number loss	de novo	See cases	Likely pathogenic	ClinVar	RCV000663385.2, VCV000548966.2	1

No genotype data were submitted for this variant

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