A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689089



Internal ID18640684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6619819..6745551hg38UCSC Ensembl
Innerchr9:6619819..6745551hg19UCSC Ensembl
Innerchr9:6609819..6735551hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38125733
hg19125733
hg18125733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023706
Supporting Variants
Samples
Known GenesGLDC, KDM4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689089
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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