A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659362



Internal ID15396014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112090912..112110551hg38UCSC Ensembl
Innerchr7:111730967..111750606hg19UCSC Ensembl
Innerchr7:111518203..111537842hg18UCSC Ensembl
Innerchr7:111324918..111344557hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3819640
hg1919640
hg1819640
hg1719640
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516034
Supporting Variants
Samples
Known GenesDOCK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659362
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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