A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1859189



Internal ID17746014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79801605..79919785hg38UCSC Ensembl
Innerchr10:81561361..81679541hg19UCSC Ensembl
Innerchr10:81543948..81669521hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38118181
hg19118181
hg18125574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948095
Supporting Variants
SamplesHGDP00521
Known GenesLOC100288974, LOC642361
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)nssv1859189
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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