A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561715



Internal ID16002438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:56224442..57213889hg38UCSC Ensembl
Innerchr13:56798576..57788023hg19UCSC Ensembl
Innerchr13:55696577..56686024hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38989448
hg19989448
hg18989448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811801
Samples
Known GenesPRR20A, PRR20B, PRR20C, PRR20D, PRR20E
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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