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dbVar

Database of genomic structural variation

nsv6290460

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:451,604

Description:GRCh37/hg19 Xq24(chrX:119448146-119899748)x2 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: 917 SVs from 59 studies. See in: genome view

Remapped(Score: Perfect):120,314,291-120,765,894

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6290460	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	120,314,291	120,765,894
nsv6290460	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	119,448,146	119,899,748

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv17956259	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV001834283.1, VCV001340748.1	2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv17956259	Remapped	Perfect	NC_000023.11:g.(?_ 120314291)_(120765 894_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	120,314,291	120,765,894
nssv17956259	Submitted genomic		NC_000023.10:g.(?_ 119448146)_(119899 748_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	119,448,146	119,899,748

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
nssv17956259	GRCh37: NC_000023.10:g.(?_119448146)_(119899748_?)dup	copy number gain	germline	not provided	Uncertain significance	ClinVar	RCV001834283.1, VCV001340748.1	2

No genotype data were submitted for this variant

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