A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522527



Internal ID8416802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:46002632..46011553hg38UCSC Ensembl
Innerchr11:46024183..46033104hg19UCSC Ensembl
Innerchr11:45980759..45989680hg18UCSC Ensembl
Innerchr11:45980759..45989680hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg388922
hg198922
hg188922
hg178922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705899
Samples
Known GenesPHF21A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522527
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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