A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950379



Internal ID17299253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:111894545..111900944hg38UCSC Ensembl
Outerchr4:112815701..112822100hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996765
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950379
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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