A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947798



Internal ID18594645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28898310..28900237hg38UCSC Ensembl
Innerchr10:29187239..29189166hg19UCSC Ensembl
Innerchr10:29227245..29229172hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381928
hg191928
hg181928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1837797, nssv1837801, nssv1837800, nssv1837794, nssv1837796, nssv1837799, nssv1837795, nssv1837803, nssv1837798, nssv1837802
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)nsv947798
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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