A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767726



Internal ID19309007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17119048..17119108hg38UCSC Ensembl
chr3:17160540..17160600hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072673
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767726
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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