A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769651



Internal ID18959941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89851991..89852592hg38UCSC Ensembl
chr16:89918399..89919000hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071317
Supporting Variants
SamplesKWP1
Known GenesSPIRE2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769651
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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