A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950406



Internal ID17299280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:137789312..137794111hg38UCSC Ensembl
Outerchr5:137125001..137129800hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997839
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950406
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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