A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975245



Internal ID18610453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134122936..134124644hg38UCSC Ensembl
Innerchr11:133992831..133994539hg19UCSC Ensembl
Innerchr11:133498041..133499749hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381709
hg191709
hg181709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1910682, nssv1910683, nssv1910687, nssv1910685, nssv1910686, nssv1910679, nssv1910688, nssv1910684, nssv1910681, nssv1910680
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesJAM3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975245
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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