A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771709



Internal ID19309059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52675832..52676171hg38UCSC Ensembl
chr3:52709848..52710187hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073644
Supporting Variants
SamplesKWP1
Known GenesPBRM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771709
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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