A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053852



Internal ID18796383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:56228152..57240122hg38UCSC Ensembl
Innerchr13:56802286..57814256hg19UCSC Ensembl
Innerchr13:55700287..56712257hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg381011971
hg191011971
hg181011971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523873
Samples
Known GenesPRR20A, PRR20B, PRR20C, PRR20D, PRR20E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053852
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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