A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689097



Internal ID18987378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6774993..7022554hg38UCSC Ensembl
Innerchr9:6774993..7022554hg19UCSC Ensembl
Innerchr9:6764993..7012554hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38247562
hg19247562
hg18247562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023461
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)nssv3689097
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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