A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948054



Internal ID18594900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69023222..69025927hg38UCSC Ensembl
Innerchr10:70782978..70785683hg19UCSC Ensembl
Innerchr10:70452984..70455689hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382706
hg192706
hg182706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1854216, nssv1854214, nssv1854217, nssv1854219, nssv1854218, nssv1854215, nssv1854221, nssv1854213, nssv1854212, nssv1854220
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)nsv948054
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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