A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2277997



Internal ID17834735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32897087..32897811hg38UCSC Ensembl
Innerchr3:32938579..32939303hg19UCSC Ensembl
Innerchr3:32913583..32914307hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38725
hg19725
hg18725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv963307
Supporting Variants
SamplesHGDP00998
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)nssv2277997
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