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dbVar

Database of genomic structural variation

nsv6308531

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:1,594

Description:nsv5556920 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: 111 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):103,525,598-103,527,191

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6308531	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	103,525,598	103,527,191
nsv6308531	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	103,166,045	103,167,638

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17650706	mobile element insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17650706	Remapped	Perfect	NC_000007.14:g.103 525598_103527191in s?	GRCh38.p12	First Pass	NC_000007.14	Chr7	103,525,598	103,527,191
nssv17650706	Submitted genomic		NC_000007.13:g.103 166045_103167638in s?	GRCh37 (hg19)		NC_000007.13	Chr7	103,166,045	103,167,638

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)
nssv17650706	0.722	4623	6404

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