A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948067



Internal ID18594913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73415030..73422793hg38UCSC Ensembl
Innerchr10:75174788..75182551hg19UCSC Ensembl
Innerchr10:74844794..74852557hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg387764
hg197764
hg187764
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1857074, nssv1857075, nssv1857077, nssv1857076, nssv1857072, nssv1857079, nssv1857078, nssv1857081, nssv1857073, nssv1857080
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)nsv948067
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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