A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516862



Internal ID15444155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13052619..13145476hg38UCSC Ensembl
Innerchr2:13192744..13285601hg19UCSC Ensembl
Innerchr2:13110195..13203052hg18UCSC Ensembl
Innerchr2:13143342..13236199hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3892858
hg1992858
hg1892858
hg1792858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661538, nssv658171, nssv692094, nssv654522, nssv655713
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516862
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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