A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946276



Internal ID18593126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:145480142..145485104hg38UCSC Ensembl
Innerchr1:145983775..145988738hg19UCSC Ensembl
Innerchr1:144695132..144700095hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg384963
hg194964
hg184964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1790688, nssv1790687, nssv1790684, nssv1790686, nssv1790685, nssv1790683, nssv1790682, nssv1790690, nssv1790681, nssv1790689
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC100288142, LOC101929780, NBPF10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946276
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