A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522395



Internal ID15449688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:159345574..159346771hg38UCSC Ensembl
Innerchr5:158772582..158773779hg19UCSC Ensembl
Innerchr5:158705160..158706357hg18UCSC Ensembl
Innerchr5:158705160..158706357hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381198
hg191198
hg181198
hg171198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694164
Samples
Known GenesLOC285626
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522395
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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