A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975953



Internal ID18611160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77867702..77870923hg38UCSC Ensembl
Innerchr11:77578748..77581969hg19UCSC Ensembl
Innerchr11:77256396..77259617hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383222
hg193222
hg183222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1897260, nssv1897265, nssv1897266, nssv1897259, nssv1897261, nssv1897262, nssv1897267, nssv1897264, nssv1897268, nssv1897263
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAAMDC
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975953
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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