A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981011



Internal ID18616210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109221106..109227066hg38UCSC Ensembl
Innerchr5:108556807..108562767hg19UCSC Ensembl
Innerchr5:108584706..108590666hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg385961
hg195961
hg185961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763861
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981011
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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