A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947948



Internal ID18248108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46292382..46301057hg38UCSC Ensembl
Innerchr10:47663618..47672293hg19UCSC Ensembl
Innerchr10:47133624..47142299hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388676
hg198676
hg188676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1854835, nssv1854828, nssv1854831, nssv1854827, nssv1854833, nssv1854829, nssv1854832, nssv1854836, nssv1854830, nssv1854834
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANTXRL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947948
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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