A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036006



Internal ID19125225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:56966623..57204234hg38UCSC Ensembl
Innerchr13:57540757..57778368hg19UCSC Ensembl
Innerchr13:56438758..56676369hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38237612
hg19237612
hg18237612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523878
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)nsv1036006
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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