A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689090



Internal ID18640685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6656619..6725007hg38UCSC Ensembl
Innerchr9:6656619..6725007hg19UCSC Ensembl
Innerchr9:6646619..6715007hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3868389
hg1968389
hg1868389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028863
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)nssv3689090
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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