A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607799



Internal ID16395208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90871801..90918505hg38UCSC Ensembl
Innerchr7:90501116..90547820hg19UCSC Ensembl
Innerchr7:90339052..90385756hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3846705
hg1946705
hg1846705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1090178
Samples
Known GenesCDK14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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