A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1869921



Internal ID17829153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121713361..121714009hg38UCSC Ensembl
Innerchr10:123472875..123473523hg19UCSC Ensembl
Innerchr10:123462865..123463513hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38649
hg19649
hg18649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948208
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)nssv1869921
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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