A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607793



Internal ID16048516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90586963..90608517hg38UCSC Ensembl
Innerchr7:90216277..90237831hg19UCSC Ensembl
Innerchr7:90054213..90075767hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3821555
hg1921555
hg1821555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11500n54
Supporting Variantsnssv1090173
Samples
Known GenesCDK14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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