A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763143



Internal ID18963631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83967394..83968795hg38UCSC Ensembl
chr16:84000999..84002400hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070361
Supporting Variants
SamplesKWP1
Known GenesNECAB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763143
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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