A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524054



Internal ID18822335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57139082..57193352hg38UCSC Ensembl
Innerchr13:57713216..57767486hg19UCSC Ensembl
Innerchr13:56611217..56665487hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3854271
hg1954271
hg1854271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052899
Supporting Variants
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)nssv3524054
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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