A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695106



Internal ID18993387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112954828..113024761hg38UCSC Ensembl
Innerchr9:115717108..115787041hg19UCSC Ensembl
Innerchr9:114756929..114826862hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3869934
hg1969934
hg1869934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052547
Supporting Variants
Samples
Known GenesZNF883
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695106
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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