A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561719



Internal ID16349128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:56979212..57331081hg38UCSC Ensembl
Innerchr13:57553346..57905215hg19UCSC Ensembl
Innerchr13:56451347..56803216hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38351870
hg19351870
hg18351870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811805, nssv811806
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)nsv561719
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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