A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1865301



Internal ID17532018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103245020..103247057hg38UCSC Ensembl
Innerchr10:105004777..105006814hg19UCSC Ensembl
Innerchr10:104994767..104996804hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg382038
hg192038
hg182038
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948175
Supporting Variants
SamplesHGDP01307
Known GenesLOC729020
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)nssv1865301
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