A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1843103



Internal ID17745268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42688178..42729123hg38UCSC Ensembl
Innerchr10:43183626..43224571hg19UCSC Ensembl
Innerchr10:42503632..42544577hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3840946
hg1940946
hg1840946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947887
Supporting Variants
SamplesHGDP00521
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)nssv1843103
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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