A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009776



Internal ID19098995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34013902..34121610hg38UCSC Ensembl
Innerchr2:34238969..34346677hg19UCSC Ensembl
Innerchr2:34092473..34200181hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38107709
hg19107709
hg18107709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3756n100
Supporting Variantsnssv3580892
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)nsv1009776
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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