A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975936



Internal ID18264457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61964459..61965666hg38UCSC Ensembl
Innerchr11:61731931..61733138hg19UCSC Ensembl
Innerchr11:61488507..61489714hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381208
hg191208
hg181208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1892609, nssv1892612, nssv1892613, nssv1892608, nssv1892616, nssv1892610, nssv1892614, nssv1892617, nssv1892611, nssv1892615
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesBEST1, FTH1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975936
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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