A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948213



Internal ID18595059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123170956..123172078hg38UCSC Ensembl
Innerchr10:124930472..124931594hg19UCSC Ensembl
Innerchr10:124920462..124921584hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381123
hg191123
hg181123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1869297, nssv1869301, nssv1869295, nssv1869302, nssv1869296, nssv1869303, nssv1869300, nssv1869298, nssv1869299, nssv1869304
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)nsv948213
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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