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dbVar

Database of genomic structural variation

nsv6129069

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:855

Description:nsv5514507 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.

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: 133 SVs from 35 studies. See in: genome view

Remapped(Score: Perfect):4,737,312-4,738,166

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6129069	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	4,737,312	4,738,166
nsv6129069	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	4,640,607	4,641,461

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17965096	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17965096	Remapped	Perfect	NC_000017.11:g.473 7312_4738166del	GRCh38.p12	First Pass	NC_000017.11	Chr17	4,737,312	4,738,166
nssv17965096	Submitted genomic		NC_000017.10:g.464 0607_4641461del	GRCh37 (hg19)		NC_000017.10	Chr17	4,640,607	4,641,461

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17965096	0.031	199	6404

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