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dbVar

Database of genomic structural variation

nsv6130074

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:16

Description:nsv5547800 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: 107 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):14,055,291-14,055,306

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6130074	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	14,055,291	14,055,306
nsv6130074	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	14,166,103	14,166,118

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17959046	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17959046	Remapped	Perfect	NC_000019.10:g.140 55291_14055306ins?	GRCh38.p12	First Pass	NC_000019.10	Chr19	14,055,291	14,055,306
nssv17959046	Submitted genomic		NC_000019.9:g.1416 6103_14166118ins?	GRCh37 (hg19)		NC_000019.9	Chr19	14,166,103	14,166,118

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)
nssv17959046	0.142	912	6404

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