A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981009



Internal ID18616208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:43101456..43114772hg38UCSC Ensembl
Innerchr5:43101558..43114874hg19UCSC Ensembl
Innerchr5:43137315..43150631hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3813317
hg1913317
hg1813317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757503
SamplesHGDP00542
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981009
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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