A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026620



Internal ID19115838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30722878..31086174hg38UCSC Ensembl
Innerchr9:30722876..31086172hg19UCSC Ensembl
Innerchr9:30712876..31076172hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38363297
hg19363297
hg18363297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688840
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)nsv1026620
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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