A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676394



Internal ID15413046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112090912..112109392hg38UCSC Ensembl
Innerchr7:111730967..111749447hg19UCSC Ensembl
Innerchr7:111518203..111536683hg18UCSC Ensembl
Innerchr7:111324918..111343398hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3818481
hg1918481
hg1818481
hg1718481
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)nssv676394
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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