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dbVar

Database of genomic structural variation

nsv6311207

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:144,658

Description:NC_000002.11:g.(?_105858316)_(106002973_?)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: 315 SVs from 44 studies. See in: genome view

Remapped(Score: Perfect):105,241,859-105,386,516

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6311207	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	105,241,859	105,386,516
nsv6311207	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	105,858,316	106,002,973

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv17974988	duplication	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV001929210.3, VCV001426062.3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv17974988	Remapped	Perfect	NC_000002.12:g.(?_ 105241859)_(105386 516_?)dup	GRCh38.p12	First Pass	NC_000002.12	Chr2	105,241,859	105,386,516
nssv17974988	Submitted genomic		NC_000002.11:g.(?_ 105858316)_(106002 973_?)dup	GRCh37 (hg19)		NC_000002.11	Chr2	105,858,316	106,002,973

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
nssv17974988	GRCh37: NC_000002.11:g.(?_105858316)_(106002973_?)dup	duplication	germline	not provided	Uncertain significance	ClinVar	RCV001929210.3, VCV001426062.3

No genotype data were submitted for this variant

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