A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762783



Internal ID18961293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88052693..88055094hg38UCSC Ensembl
chr16:88086299..88088700hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077833
Supporting Variants
SamplesKWP1
Known GenesBANP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762783
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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