A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947861



Internal ID18594708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38458555..38529907hg38UCSC Ensembl
Innerchr10:38747483..38818835hg19UCSC Ensembl
Innerchr10:38787489..38859132hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3871353
hg1971353
hg1871644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv21n82
Supporting Variantsnssv1842560, nssv1842561, nssv1842556, nssv1842562, nssv1842555, nssv1842564, nssv1842558, nssv1842557, nssv1842559, nssv1842563
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)nsv947861
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