A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2523753



Internal ID17394058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19105114..19108547hg38UCSC Ensembl
Innerchr9:19105112..19108545hg19UCSC Ensembl
Innerchr9:19095112..19098545hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg383434
hg193434
hg183434
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982198
Supporting Variants
SamplesHGDP00456
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)nssv2523753
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