A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1090177



Internal ID15943363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90783597..90819060hg38UCSC Ensembl
Innerchr7:90412912..90448375hg19UCSC Ensembl
Innerchr7:90250848..90286311hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3835464
hg1935464
hg1835464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607798
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)nssv1090177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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