A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671379



Internal ID15061345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181187665..181206954hg38UCSC Ensembl
Innerchr5:180614665..180633954hg19UCSC Ensembl
Innerchr5:180547271..180566560hg18UCSC Ensembl
Innerchr5:180547271..180566560hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3819290
hg1919290
hg1819290
hg1719290
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517697
Supporting Variants
Samples
Known GenesLOC102577426, TRIM7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671379
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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