A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689096



Internal ID18987377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6731786..7372132hg38UCSC Ensembl
Innerchr9:6731786..7372132hg19UCSC Ensembl
Innerchr9:6721786..7362132hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38640347
hg19640347
hg18640347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023906
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)nssv3689096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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