A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525166



Internal ID15105773
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701240
Samples
Known GenesATP10B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525166
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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