A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607796



Internal ID16395205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90770544..90805716hg38UCSC Ensembl
Innerchr7:90399859..90435031hg19UCSC Ensembl
Innerchr7:90237795..90272967hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3835173
hg1935173
hg1835173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1090175
Samples
Known GenesCDK14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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