A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948227



Internal ID18595073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130105923..130108469hg38UCSC Ensembl
Innerchr10:131904187..131906733hg19UCSC Ensembl
Innerchr10:131794177..131796723hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382547
hg192547
hg182547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1869881, nssv1869873, nssv1869880, nssv1869882, nssv1869876, nssv1869879, nssv1869878, nssv1869874, nssv1869877, nssv1869875
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCTAGE7P, LINC00959
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948227
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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