A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971344



Internal ID18606564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105010259..105016625hg38UCSC Ensembl
Innerchr8:106022487..106028853hg19UCSC Ensembl
Innerchr8:106091663..106098029hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg386367
hg196367
hg186367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2515724, nssv2515720, nssv2515718, nssv2515723, nssv2515716, nssv2515719, nssv2515715, nssv2515722, nssv2515717, nssv2515721
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971344
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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