A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948171



Internal ID18595017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102845587..102854090hg38UCSC Ensembl
Innerchr10:104605344..104613847hg19UCSC Ensembl
Innerchr10:104595334..104603837hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg388504
hg198504
hg188504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1864389, nssv1864394, nssv1864386, nssv1864387, nssv1864391, nssv1864390, nssv1864385, nssv1864392, nssv1864388, nssv1864393
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)nsv948171
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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