A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983042



Internal ID18618236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72940461..72940961hg38UCSC Ensembl
Innerchr11:72651506..72652006hg19UCSC Ensembl
Innerchr11:72329154..72329654hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1895326, nssv1895330, nssv1895323, nssv1895327, nssv1895321, nssv1895324, nssv1895328, nssv1895322, nssv1895329, nssv1895325
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFCHSD2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983042
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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