A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2559891



Internal ID17539559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92803763..92826683hg38UCSC Ensembl
Innerchr9:95566045..95588965hg19UCSC Ensembl
Innerchr9:94605866..94628786hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3822921
hg1922921
hg1822921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972420
Supporting Variants
SamplesHGDP01307
Known GenesANKRD19P
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)nssv2559891
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