A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767430



Internal ID18965832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33556219..33556554hg38UCSC Ensembl
chr2:33781286..33781621hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072406
Supporting Variants
SamplesKWP1
Known GenesRASGRP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767430
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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