A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1868509



Internal ID17829083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114118510..114119115hg38UCSC Ensembl
Innerchr10:115878269..115878874hg19UCSC Ensembl
Innerchr10:115868259..115868864hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38606
hg19606
hg18606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948191
Supporting Variants
SamplesHGDP00998
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)nssv1868509
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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