A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998214



Internal ID17291166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:43793465..43805364hg38UCSC Ensembl
Outerchr13:44367601..44379500hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951077
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998214
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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