A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092725



Internal ID15945911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111433654..112154313hg38UCSC Ensembl
Innerchr7:111073710..111794368hg19UCSC Ensembl
Innerchr7:110860946..111581604hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38720660
hg19720659
hg18720659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608196
Supporting Variants
Samples
Known GenesDOCK4, DOCK4-AS1, IMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092725
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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