A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771835



Internal ID18967233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139934857..139935758hg38UCSC Ensembl
chr3:139653699..139654600hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073684
Supporting Variants
SamplesKWP1
Known GenesCLSTN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771835
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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