A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947901



Internal ID18594748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44478660..44505278hg38UCSC Ensembl
Innerchr10:44974108..45000726hg19UCSC Ensembl
Innerchr10:44294114..44320732hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3826619
hg1926619
hg1826619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1844610, nssv1844606, nssv1844607, nssv1844608, nssv1844609, nssv1844602, nssv1844611, nssv1844604, nssv1844605, nssv1844603
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)nsv947901
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