A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000200



Internal ID17293152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:90098993..90166792hg38UCSC Ensembl
Outerchr16:90165401..90233200hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3867800
hg1967800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952081
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000200
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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