A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967633



Internal ID18602861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133755037..133760761hg38UCSC Ensembl
Innerchr8:134767280..134773004hg19UCSC Ensembl
Innerchr8:134836462..134842186hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg385725
hg195725
hg185725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2519060, nssv2519059, nssv2519063, nssv2519061, nssv2519056, nssv2519062, nssv2519057, nssv2519064, nssv2519058, nssv2519055
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)nsv967633
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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