A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2565621



Internal ID17806892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112496667..112498047hg38UCSC Ensembl
Innerchr9:115258947..115260327hg19UCSC Ensembl
Innerchr9:114298768..114300148hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381381
hg191381
hg181381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972801
Supporting Variants
SamplesHGDP00778
Known GenesKIAA1958
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)nssv2565621
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