A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948156



Internal ID18595002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97307959..97312391hg38UCSC Ensembl
Innerchr10:99067716..99072148hg19UCSC Ensembl
Innerchr10:99057706..99062138hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg384433
hg194433
hg184433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1864681, nssv1864676, nssv1864679, nssv1864674, nssv1864677, nssv1864675, nssv1864673, nssv1864678, nssv1864672, nssv1864680
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)nsv948156
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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