A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701068



Internal ID15437720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:30845358..30916926hg38UCSC Ensembl
Innerchr5:30845465..30917033hg19UCSC Ensembl
Innerchr5:30881222..30952790hg18UCSC Ensembl
Innerchr5:30881222..30952790hg17UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3871569
hg1971569
hg1871569
hg1771569
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525028
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701068
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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