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dbVar

Database of genomic structural variation

nsv4676090

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:617,591

Description:GRCh37/hg19 5q12.1(chr5:61432724-62050314)x3 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: 1819 SVs from 87 studies. See in: genome view

Remapped(Score: Perfect):62,136,897-62,754,487

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4676090	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	62,136,897	62,754,487
nsv4676090	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	61,432,724	62,050,314

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv16206766	copy number gain	Multiple	Multiple	not provided	Likely benign	ClinVar	RCV001005680.1, VCV000814690.1	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16206766	Remapped	Perfect	NC_000005.10:g.(?_ 62136897)_(6275448 7_?)dup	GRCh38.p12	First Pass	NC_000005.10	Chr5	62,136,897	62,754,487
nssv16206766	Submitted genomic		NC_000005.9:g.(?_6 1432724)_(62050314 _?)dup	GRCh37 (hg19)		NC_000005.9	Chr5	61,432,724	62,050,314

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
nssv16206766	GRCh37: NC_000005.9:g.(?_61432724)_(62050314_?)dup	copy number gain	germline	not provided	Likely benign	ClinVar	RCV001005680.1, VCV000814690.1	3

No genotype data were submitted for this variant

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