A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701435



Internal ID15438087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25521176..25537306hg38UCSC Ensembl
Innerchr5:25521285..25537415hg19UCSC Ensembl
Innerchr5:25557042..25573172hg18UCSC Ensembl
Innerchr5:25557042..25573172hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3816131
hg1916131
hg1816131
hg1716131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525325
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701435
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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