A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527056



Internal ID8421331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67439955..67526837hg38UCSC Ensembl
Innerchr11:67207426..67294308hg19UCSC Ensembl
Innerchr11:66964002..67050884hg18UCSC Ensembl
Innerchr11:66964002..67050884hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3886883
hg1986883
hg1886883
hg1786883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703432
Samples
Known GenesAIP, CABP2, CABP4, CDK2AP2, CORO1B, GPR152, MIR6752, PITPNM1, TMEM134
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527056
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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