A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011569



Internal ID19100786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34013902..34093335hg38UCSC Ensembl
Innerchr2:34238969..34318402hg19UCSC Ensembl
Innerchr2:34092473..34171906hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3879434
hg1979434
hg1879434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3756n100
Supporting Variantsnssv3580891
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011569
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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