A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020052



Internal ID19109271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25718006..25737728hg38UCSC Ensembl
Innerchr9:25718004..25737726hg19UCSC Ensembl
Innerchr9:25708004..25727726hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3819723
hg1919723
hg1819723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691986
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)nsv1020052
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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