A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126848



Internal ID15980034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7015330..7037370hg38UCSC Ensembl
Innerchr9:7015330..7037370hg19UCSC Ensembl
Innerchr9:7005330..7027370hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3822041
hg1922041
hg1822041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613257
Supporting Variants
Samples
Known GenesKDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126848
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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