A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1854834



Internal ID17498368
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 StatusS
Merged Variantsnsv947948
Supporting Variants
SamplesHGDP01029
Known GenesANTXRL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1854834
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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