A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2566998



Internal ID17528947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130458369..130459908hg38UCSC Ensembl
Innerchr9:133333756..133335295hg19UCSC Ensembl
Innerchr9:132323577..132325116hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381540
hg191540
hg181540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972455
Supporting Variants
SamplesHGDP01284
Known GenesASS1
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)nssv2566998
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