A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1851796



Internal ID17844912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52410958..52414225hg38UCSC Ensembl
Innerchr10:54170718..54173985hg19UCSC Ensembl
Innerchr10:53840724..53843991hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg383268
hg193268
hg183268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948011
Supporting Variants
SamplesHGDP01029
Known Genes
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)nssv1851796
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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