A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952237



Internal ID17301111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:100057364..100067263hg38UCSC Ensembl
Outerchr14:100523701..100533600hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998397
SamplesBILGI_BIOE
Known GenesEVL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952237
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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