A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518269



Internal ID15445562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:94608113..94613965hg38UCSC Ensembl
Innerchr5:93943818..93949670hg19UCSC Ensembl
Innerchr5:93969574..93975426hg18UCSC Ensembl
Innerchr5:93969574..93975426hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg385853
hg195853
hg185853
hg175853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695700
Samples
Known GenesKIAA0825
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518269
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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