A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950630



Internal ID17299504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:1526886..1537485hg38UCSC Ensembl
Outerchr5:1527001..1537600hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997688
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950630
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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