A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951912



Internal ID17300786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:103640251..103645150hg38UCSC Ensembl
Outerchr13:104292601..104297500hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998252
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951912
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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