A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975176



Internal ID18263698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49151185..49164740hg38UCSC Ensembl
Innerchr11:49172737..49186292hg19UCSC Ensembl
Innerchr11:49129313..49142868hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3813556
hg1913556
hg1813556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1885809, nssv1885813, nssv1885810, nssv1885814, nssv1885808, nssv1885807, nssv1885815, nssv1885811, nssv1885806, nssv1885812
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFOLH1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975176
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