A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524005



Internal ID18822286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57138666..57204234hg38UCSC Ensembl
Innerchr13:57712800..57778368hg19UCSC Ensembl
Innerchr13:56610801..56676369hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3865569
hg1965569
hg1865569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052518
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)nssv3524005
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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