A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764133



Internal ID19309643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64252327..64253128hg38UCSC Ensembl
chr11:64019799..64020600hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070965
Supporting Variants
SamplesKWP1
Known GenesPLCB3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764133
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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