A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947920



Internal ID18248080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45928109..45931516hg38UCSC Ensembl
Innerchr10:46423557..46426964hg19UCSC Ensembl
Innerchr10:45743563..45747193hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383408
hg193408
hg183631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1846631, nssv1846633, nssv1846628, nssv1846629, nssv1846634, nssv1846632, nssv1846627, nssv1846635, nssv1846630, nssv1846626
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)nsv947920
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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