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dbVar

Database of genomic structural variation

nsv7094912

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:137

Description:NC_000017.10:g.(?_63149520)_(63149656_?)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: 89 SVs from 13 studies. See in: genome view

Remapped(Score: Perfect):65,153,402-65,153,538

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7094912	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	65,153,402	65,153,538
nsv7094912	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	63,149,520	63,149,656

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18788317	duplication	Multiple	Multiple	not provided	Likely pathogenic	ClinVar	RCV003107758.2, VCV002424775.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18788317	Remapped	Perfect	NC_000017.11:g.(?_ 65153402)_(6515353 8_?)dup	GRCh38.p12	First Pass	NC_000017.11	Chr17	65,153,402	65,153,538
nssv18788317	Submitted genomic		NC_000017.10:g.(?_ 63149520)_(6314965 6_?)dup	GRCh37 (hg19)		NC_000017.10	Chr17	63,149,520	63,149,656

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
nssv18788317	GRCh37: NC_000017.10:g.(?_63149520)_(63149656_?)dup	duplication	germline	not provided	Likely pathogenic	ClinVar	RCV003107758.2, VCV002424775.2

No genotype data were submitted for this variant

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