A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522905



Internal ID15450198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166471277..166482446hg38UCSC Ensembl
Innerchr6:166884765..166895934hg19UCSC Ensembl
Innerchr6:166804755..166815924hg18UCSC Ensembl
Innerchr6:166855176..166866345hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3811170
hg1911170
hg1811170
hg1711170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv400n21
Supporting Variantsnssv698563
Samples
Known GenesRPS6KA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522905
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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