A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526571



Internal ID18824852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57545587..57714368hg38UCSC Ensembl
Innerchr13:58119721..58288502hg19UCSC Ensembl
Innerchr13:57017722..57186503hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38168782
hg19168782
hg18168782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044463
Supporting Variants
Samples
Known GenesPCDH17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526571
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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