A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945766



Internal ID18592617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10052471..10055171hg38UCSC Ensembl
Innerchr1:10112529..10115229hg19UCSC Ensembl
Innerchr1:10035116..10037816hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382701
hg192701
hg182701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1754817, nssv1754812, nssv1754813, nssv1754820, nssv1754814, nssv1754819, nssv1754818, nssv1754816, nssv1754821, nssv1754815
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesUBE4B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945766
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