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dbVar

Database of genomic structural variation

nsv7096070

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:263,111

Description:NC_000020.10:g.(?_25056897)_(25320007_?)dup AND not provided

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: 722 SVs from 63 studies. See in: genome view

Remapped(Score: Perfect):25,076,261-25,339,371

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7096070	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	25,076,261	25,339,371
nsv7096070	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000020.10	Chr20	25,056,897	25,320,007

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18787416	duplication	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV003122408.1, VCV002423578.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18787416	Remapped	Perfect	NC_000020.11:g.(?_ 25076261)_(2533937 1_?)dup	GRCh38.p12	First Pass	NC_000020.11	Chr20	25,076,261	25,339,371
nssv18787416	Submitted genomic		NC_000020.10:g.(?_ 25056897)_(2532000 7_?)dup	GRCh37 (hg19)		NC_000020.10	Chr20	25,056,897	25,320,007

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
nssv18787416	GRCh37: NC_000020.10:g.(?_25056897)_(25320007_?)dup	duplication	germline	not provided	Uncertain significance	ClinVar	RCV003122408.1, VCV002423578.2

No genotype data were submitted for this variant

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