A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1090176



Internal ID15943362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90782827..90805716hg38UCSC Ensembl
Innerchr7:90412142..90435031hg19UCSC Ensembl
Innerchr7:90250078..90272967hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3822890
hg1922890
hg1822890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607797
Supporting Variants
Samples
Known GenesCDK14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1090176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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