A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1859558



Internal ID17498640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79630499..79715283hg38UCSC Ensembl
Innerchr10:81390255..81475039hg19UCSC Ensembl
Innerchr10:81060261..81145045hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3884785
hg1984785
hg1884785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948085
Supporting Variants
SamplesHGDP01029
Known GenesBEND3P3, NUTM2B
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)nssv1859558
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