A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1851590



Internal ID17390264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67793738..67796718hg38UCSC Ensembl
Innerchr10:69553496..69556476hg19UCSC Ensembl
Innerchr10:69223502..69226482hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382981
hg192981
hg182981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948043
Supporting Variants
SamplesHGDP00456
Known GenesDNAJC12
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)nssv1851590
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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