A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661159



Internal ID15397811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112090912..112110579hg38UCSC Ensembl
Innerchr7:111730967..111750634hg19UCSC Ensembl
Innerchr7:111518203..111537870hg18UCSC Ensembl
Innerchr7:111324918..111344585hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3819668
hg1919668
hg1819668
hg1719668
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)nssv661159
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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