A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1861832



Internal ID17779124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87068831..87085866hg38UCSC Ensembl
Innerchr10:88828588..88845623hg19UCSC Ensembl
Innerchr10:88818568..88835603hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3817036
hg1917036
hg1817036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948113
Supporting Variants
SamplesHGDP00665
Known GenesGLUD1
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)nssv1861832
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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