A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1090174



Internal ID15596674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90586963..90610884hg38UCSC Ensembl
Innerchr7:90216277..90240198hg19UCSC Ensembl
Innerchr7:90054213..90078134hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3823922
hg1923922
hg1823922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607794
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)nssv1090174
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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