A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948072



Internal ID18248232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74525280..74530420hg38UCSC Ensembl
Innerchr10:76285038..76290178hg19UCSC Ensembl
Innerchr10:75955044..75960184hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg385141
hg195141
hg185141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1857560, nssv1857559, nssv1857554, nssv1857557, nssv1857556, nssv1857551, nssv1857558, nssv1857553, nssv1857552, nssv1857555
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesADK
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948072
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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