A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764639



Internal ID18962103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89618791..89619892hg38UCSC Ensembl
chr16:89685199..89686300hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071350
Supporting Variants
SamplesKWP1
Known GenesDPEP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764639
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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