A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521367



Internal ID15448660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55218805..57477258hg38UCSC Ensembl
Innerchr13:55792940..58051392hg19UCSC Ensembl
Innerchr13:54690941..56949393hg18UCSC Ensembl
Innerchr13:54690941..56949393hg17UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg382258454
hg192258453
hg182258453
hg172258453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697977
Samples
Known GenesPRR20A, PRR20B, PRR20C, PRR20D, PRR20E
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521367
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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