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dbVar

Database of genomic structural variation

nsv6308831

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:52

Description:nsv5554652 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: 182 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):103,822,215-103,822,266

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6308831	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	103,822,215	103,822,266
nsv6308831	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	104,834,443	104,834,494

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17653790	line1 insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17653790	Remapped	Perfect	NC_000008.11:g.103 822215_103822266in s?	GRCh38.p12	First Pass	NC_000008.11	Chr8	103,822,215	103,822,266
nssv17653790	Submitted genomic		NC_000008.10:g.104 834443_104834494in s?	GRCh37 (hg19)		NC_000008.10	Chr8	104,834,443	104,834,494

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)
nssv17653790	0.015	95	6404

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