A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771504



Internal ID19308026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54430587..54432488hg38UCSC Ensembl
chr16:54464499..54466400hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071290
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771504
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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