A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689092



Internal ID18640687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6669375..6741529hg38UCSC Ensembl
Innerchr9:6669375..6741529hg19UCSC Ensembl
Innerchr9:6659375..6731529hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3872155
hg1972155
hg1872155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030278
Supporting Variants
Samples
Known GenesKDM4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689092
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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