A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1832495



Internal ID17447603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13317887..13320070hg38UCSC Ensembl
Innerchr10:13359887..13362070hg19UCSC Ensembl
Innerchr10:13399893..13402076hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382184
hg192184
hg182184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947742
Supporting Variants
SamplesHGDP00778
Known GenesSEPHS1
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)nssv1832495
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