A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975219



Internal ID18610427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92497829..92499814hg38UCSC Ensembl
Innerchr11:92230995..92232980hg19UCSC Ensembl
Innerchr11:91870643..91872628hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381986
hg191986
hg181986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901158, nssv1901157, nssv1901159, nssv1901156, nssv1901155, nssv1901160, nssv1901161, nssv1901164, nssv1901163, nssv1901162
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAT3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975219
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer