A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948073



Internal ID18594919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75088061..75092700hg38UCSC Ensembl
Innerchr10:76847819..76852458hg19UCSC Ensembl
Innerchr10:76517825..76522464hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg384640
hg194640
hg184640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1857652, nssv1857655, nssv1857649, nssv1857657, nssv1857653, nssv1857650, nssv1857648, nssv1857654, nssv1857656, nssv1857651
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)nsv948073
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