A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953936



Internal ID17302810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:151901..184800hg38UCSC Ensembl
Outerchr19:151901..184800hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3832900
hg1932900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998915
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953936
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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