A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950391



Internal ID17299265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:132419809..132428008hg38UCSC Ensembl
Outerchr5:131755501..131763700hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997824
SamplesBILGI_BIOE
Known GenesC5orf56
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950391
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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