A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948140



Internal ID18594986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92668566..92676396hg38UCSC Ensembl
Innerchr10:94428323..94436153hg19UCSC Ensembl
Innerchr10:94418303..94426133hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg387831
hg197831
hg187831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865414, nssv1865415, nssv1865420, nssv1865421, nssv1865417, nssv1865413, nssv1865418, nssv1865416, nssv1865422, nssv1865419
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)nsv948140
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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