A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967549



Internal ID18602777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98143..163030hg38UCSC Ensembl
Innerchr8:48143..113030hg19UCSC Ensembl
Innerchr8:38143..103030hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3864888
hg1964888
hg1864888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2488919, nssv2488922, nssv2488926, nssv2488918, nssv2488920, nssv2488917, nssv2488924, nssv2488921, nssv2488925, nssv2488923
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)nsv967549
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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