A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1861005



Internal ID17878508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86630093..86632568hg38UCSC Ensembl
Innerchr10:88389850..88392325hg19UCSC Ensembl
Innerchr10:88379830..88382305hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382476
hg192476
hg182476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948110
Supporting Variants
SamplesHGDP01307
Known Genes
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)nssv1861005
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