A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1837105



Internal ID17389604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29570238..29571335hg38UCSC Ensembl
Innerchr10:29859167..29860264hg19UCSC Ensembl
Innerchr10:29899173..29900270hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381098
hg191098
hg181098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947805
Supporting Variants
SamplesHGDP00456
Known GenesSVIL
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)nssv1837105
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