A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000127



Internal ID17293079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:35915330..36041429hg38UCSC Ensembl
Outerchr16:35149701..35275800hg19UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38126100
hg19126100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952660
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000127
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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