A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982981



Internal ID18618175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9094016..9099804hg38UCSC Ensembl
Innerchr11:9115563..9121351hg19UCSC Ensembl
Innerchr11:9072139..9077927hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385789
hg195789
hg185789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1875536, nssv1875538, nssv1875543, nssv1875541, nssv1875537, nssv1875539, nssv1875540, nssv1875544, nssv1875535, nssv1875542
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKRT8P41
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982981
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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