A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2306624



Internal ID17749174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182460156..182460656hg38UCSC Ensembl
Innerchr3:182177944..182178444hg19UCSC Ensembl
Innerchr3:183660638..183661138hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv963385
Supporting Variants
SamplesHGDP00521
Known GenesFLJ46066
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)nssv2306624
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