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dbVar

Database of genomic structural variation

nsv5393469

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:6,231

Description:nsv5036275 from Abel et. al 2020. 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: 148 SVs from 49 studies. See in: genome view

Remapped(Score: Perfect):19,764,893-19,771,123

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5393469	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	19,764,893	19,771,123
nsv5393469	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	19,765,124	19,771,354

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16875331	line1 deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16875331	Remapped	Perfect	NC_000006.12:g.197 64893_19771123del	GRCh38.p12	First Pass	NC_000006.12	Chr6	19,764,893	19,771,123
nssv16875331	Submitted genomic		NC_000006.11:g.197 65124_19771354del	GRCh37 (hg19)		NC_000006.11	Chr6	19,765,124	19,771,354

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)
nssv16875331	0.541	15834	29246

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