A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982124



Internal ID18617320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:24282642..24293949hg38UCSC Ensembl
Innerchr8:24140155..24151462hg19UCSC Ensembl
Innerchr8:24196100..24207407hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3811308
hg1911308
hg1811308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758923, nssv2762967, nssv2765712
SamplesHGDP00542, HGDP01029, HGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982124
Frequency
Sample Size10
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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