A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690713



Internal ID18642308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21455761..21524675hg38UCSC Ensembl
Innerchr9:21455760..21524674hg19UCSC Ensembl
Innerchr9:21445760..21514674hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3868915
hg1968915
hg1868915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030064
Supporting Variants
Samples
Known GenesIFNE, MIR31, MIR31HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690713
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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