A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765698



Internal ID18966072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236567456..236568357hg38UCSC Ensembl
chr2:237476099..237477000hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073025
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765698
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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