A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689241



Internal ID18987522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11600297..11802691hg38UCSC Ensembl
Innerchr9:11600297..11802691hg19UCSC Ensembl
Innerchr9:11590297..11792691hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38202395
hg19202395
hg18202395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023172
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)nssv3689241
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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