A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516034



Internal ID15443091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112090912..112119529hg38UCSC Ensembl
Innerchr7:111730967..111759584hg19UCSC Ensembl
Innerchr7:111518203..111546820hg18UCSC Ensembl
Innerchr7:111324918..111353535hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3828618
hg1928618
hg1828618
hg1728618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665845, nssv661159, nssv659362, nssv663451, nssv676394
Samples
Known GenesDOCK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516034
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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