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dbVar

Database of genomic structural variation

nsv4724824

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:1

Description:nsv4533271 from gnomAD Structural Variants. 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: 118 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):155,017,347-155,017,347

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4724824	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	155,017,347	155,017,347
nsv4724824	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	154,989,823	154,989,823

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16224864	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16224864	Remapped	Perfect	NC_000001.11:g.155 017347_155017348in s?	GRCh38.p12	First Pass	NC_000001.11	Chr1	155,017,347	155,017,347
nssv16224864	Submitted genomic		NC_000001.10:g.154 989823_154989824in s?	GRCh37 (hg19)		NC_000001.10	Chr1	154,989,823	154,989,823

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)
nssv16224864	0.18	3899	21676

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