A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1853893



Internal ID17522958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46266635..46283677hg38UCSC Ensembl
Innerchr10:47637871..47654913hg19UCSC Ensembl
Innerchr10:47107877..47124919hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3817043
hg1917043
hg1817043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947947
Supporting Variants
SamplesHGDP01284
Known GenesANTXRLP1
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)nssv1853893
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