A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1866675



Internal ID17829001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102571194..102575736hg38UCSC Ensembl
Innerchr10:104330951..104335493hg19UCSC Ensembl
Innerchr10:104320941..104325483hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg384543
hg194543
hg184543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948170
Supporting Variants
SamplesHGDP00998
Known GenesSUFU
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)nssv1866675
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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