A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766925



Internal ID18968747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67668628..67670029hg38UCSC Ensembl
chr11:67436099..67437500hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078326
Supporting Variants
SamplesKWP1
Known GenesALDH3B2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766925
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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