A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998219



Internal ID16944485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:50072065..50085464hg38UCSC Ensembl
Outerchr13:50646201..50659600hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951082
Supporting Variants
SamplesBILGI_BIOE
Known GenesDLEU1, DLEU2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998219
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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