A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948132



Internal ID18594978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89786423..89790925hg38UCSC Ensembl
Innerchr10:91546180..91550682hg19UCSC Ensembl
Innerchr10:91536160..91540662hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384503
hg194503
hg184503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1862439, nssv1862443, nssv1862437, nssv1862436, nssv1862438, nssv1862441, nssv1862442, nssv1862440, nssv1862435, nssv1862444
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)nsv948132
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer