A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947800



Internal ID18247961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29484380..29485607hg38UCSC Ensembl
Innerchr10:29773309..29774536hg19UCSC Ensembl
Innerchr10:29813315..29814542hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381228
hg191228
hg181228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1838919, nssv1838917, nssv1838913, nssv1838921, nssv1838912, nssv1838914, nssv1838915, nssv1838916, nssv1838920, nssv1838918
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesSVIL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947800
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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