A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953990



Internal ID17302864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15904191..15911990hg38UCSC Ensembl
Outerchr19:16015001..16022800hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998966
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953990
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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