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dbVar

Database of genomic structural variation

nsv4916935

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:1,380

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: 132 SVs from 25 studies. See in: genome view

Submitted genomic219,262,928-219,264,311

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4916935	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	219,262,930 (-2, +76)	219,264,309 (-77, +2)
nsv4916935	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	220,127,652 (-2, +76)	220,129,031 (-77, +2)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16440540	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16440540	Submitted genomic		NC_000002.12:g.(21 9262928_219263006) _(219264232_219264 311)del	GRCh38 (hg38)		NC_000002.12	Chr2	219,262,930 (-2, +76)	219,264,309 (-77, +2)
nssv16440540	Remapped	Perfect	NC_000002.11:g.(22 0127650_220127728) _(220128954_220129 033)del	GRCh37.p13	First Pass	NC_000002.11	Chr2	220,127,652 (-2, +76)	220,129,031 (-77, +2)

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)
nssv16440540	<0.001	1	29246

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