A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983069



Internal ID18271577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123057251..123060217hg38UCSC Ensembl
Innerchr11:122927959..122930925hg19UCSC Ensembl
Innerchr11:122433169..122436135hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382967
hg192967
hg182967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1908418, nssv1908427, nssv1908426, nssv1908424, nssv1908422, nssv1908425, nssv1908423, nssv1908421, nssv1908419, nssv1908420
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesHSPA8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983069
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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