A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948170



Internal ID18595016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102571194..102575736hg38UCSC Ensembl
Innerchr10:104330951..104335493hg19UCSC Ensembl
Innerchr10:104320941..104325483hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg384543
hg194543
hg184543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1866680, nssv1866678, nssv1866674, nssv1866677, nssv1866673, nssv1866681, nssv1866675, nssv1866676, nssv1866679, nssv1866672
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSUFU
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948170
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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