A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1842563



Internal ID17778212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38458555..38529907hg38UCSC Ensembl
Innerchr10:38747483..38818835hg19UCSC Ensembl
Innerchr10:38787489..38859132hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3871353
hg1971353
hg1871644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947861
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1842563
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer