A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690848



Internal ID18989129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24644780..24764076hg38UCSC Ensembl
Innerchr9:24644778..24764074hg19UCSC Ensembl
Innerchr9:24634778..24754074hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38119297
hg19119297
hg18119297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027298
Supporting Variants
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)nssv3690848
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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