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dbVar

Database of genomic structural variation

nsv4729129

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:666,258

Description:GRCh37/hg19 5p13.3-13.2(chr5:33501565-34167822)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: 1741 SVs from 84 studies. See in: genome view

Remapped(Score: Perfect):33,501,460-34,167,717

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4729129	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	33,501,460	34,167,717
nsv4729129	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	33,501,565	34,167,822

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv16254974	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV001258683.1, VCV000979507.1	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16254974	Remapped	Perfect	NC_000005.10:g.(?_ 33501460)_(3416771 7_?)dup	GRCh38.p12	First Pass	NC_000005.10	Chr5	33,501,460	34,167,717
nssv16254974	Submitted genomic		NC_000005.9:g.(?_3 3501565)_(34167822 _?)dup	GRCh37 (hg19)		NC_000005.9	Chr5	33,501,565	34,167,822

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
nssv16254974	GRCh37: NC_000005.9:g.(?_33501565)_(34167822_?)dup	copy number gain	germline	not provided	Uncertain significance	ClinVar	RCV001258683.1, VCV000979507.1	3

No genotype data were submitted for this variant

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