A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701240



Internal ID15091206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160770914..160771873hg38UCSC Ensembl
Innerchr5:160197921..160198880hg19UCSC Ensembl
Innerchr5:160130499..160131458hg18UCSC Ensembl
Innerchr5:160130499..160131458hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38960
hg19960
hg18960
hg17960
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525166
Supporting Variants
Samples
Known GenesATP10B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701240
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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