A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766140



Internal ID18962882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23944608..23946109hg38UCSC Ensembl
chr3:23986099..23987600hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073208
Supporting Variants
SamplesKWP1
Known GenesNR1D2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766140
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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