A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947978



Internal ID18594824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49430930..49441372hg38UCSC Ensembl
Innerchr10:50638976..50649418hg19UCSC Ensembl
Innerchr10:50308982..50319424hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3810443
hg1910443
hg1810443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1847685, nssv1847678, nssv1847684, nssv1847686, nssv1847681, nssv1847682, nssv1847679, nssv1847683, nssv1847680, nssv1847677
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947978
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