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dbVar

Database of genomic structural variation

nsv4931565

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:3,440

Publication(s):Abel et al. 2020

Links to Other Resources

Overlapping Genes

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: 94 SVs from 29 studies. See in: genome view

Submitted genomic54,571,235-54,574,674

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4931565	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	54,571,235 (+115)	54,574,674 (-110)
nsv4931565	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	53,867,065 (+115)	53,870,504 (-110)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16467298	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16467298	Submitted genomic		NC_000005.10:g.(?_ 54571350)_(5457456 4_?)del	GRCh38 (hg38)		NC_000005.10	Chr5	54,571,235 (+115)	54,574,674 (-110)
nssv16467298	Remapped	Perfect	NC_000005.9:g.(?_5 3867180)_(53870394 _?)del	GRCh37.p13	First Pass	NC_000005.9	Chr5	53,867,065 (+115)	53,870,504 (-110)

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)
nssv16467298	<0.001	1	29246

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