A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975935



Internal ID18264456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61795767..61796411hg38UCSC Ensembl
Innerchr11:61563239..61563883hg19UCSC Ensembl
Innerchr11:61319815..61320459hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38645
hg19645
hg18645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1891723, nssv1891721, nssv1891727, nssv1891722, nssv1891724, nssv1891728, nssv1891720, nssv1891725, nssv1891719, nssv1891726
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFEN1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975935
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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