A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766589



Internal ID18968339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138753010..138753911hg38UCSC Ensembl
chr5:138088699..138089600hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074873
Supporting Variants
SamplesKWP1
Known GenesCTNNA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766589
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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