A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770912



Internal ID18965237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26476331..26477132hg38UCSC Ensembl
chr2:26699199..26700000hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071984
Supporting Variants
SamplesKWP1
Known GenesOTOF
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770912
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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