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dbVar

Database of genomic structural variation

nsv7093367

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:5,470

Description:GRCh37/hg19 6p21.33(chr6:32006200-32011669)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: 379 SVs from 53 studies. See in: genome view

Remapped(Score: Perfect):32,038,423-32,043,892

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7093367	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	32,038,423	32,043,892
nsv7093367	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	32,006,200	32,011,669

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv18786384	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV002512326.3, VCV001879681.4	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18786384	Remapped	Perfect	NC_000006.12:g.(?_ 32038423)_(3204389 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	32,038,423	32,043,892
nssv18786384	Submitted genomic		NC_000006.11:g.(?_ 32006200)_(3201166 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	32,006,200	32,011,669

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
nssv18786384	GRCh37: NC_000006.11:g.(?_32006200)_(32011669_?)dup	copy number gain	germline	not provided	Uncertain significance	ClinVar	RCV002512326.3, VCV001879681.4	3

No genotype data were submitted for this variant

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