A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021469



Internal ID19110686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31614033..31649982hg38UCSC Ensembl
Innerchr9:31614031..31649980hg19UCSC Ensembl
Innerchr9:31604031..31639980hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3835950
hg1935950
hg1835950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688859
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)nsv1021469
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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