A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690700



Internal ID18988981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20269303..20287141hg38UCSC Ensembl
Innerchr9:20269301..20287139hg19UCSC Ensembl
Innerchr9:20259301..20277139hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3817839
hg1917839
hg1817839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016273
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)nssv3690700
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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