A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1866733



Internal ID17795945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117192661..117196669hg38UCSC Ensembl
Innerchr10:118952172..118956180hg19UCSC Ensembl
Innerchr10:118942162..118946170hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg384009
hg194009
hg184009
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948197
Supporting Variants
SamplesHGDP00778
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)nssv1866733
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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