A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2561886



Internal ID17773585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96780038..96786124hg38UCSC Ensembl
Innerchr9:99542320..99548406hg19UCSC Ensembl
Innerchr9:98582141..98588227hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386087
hg196087
hg186087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972429
Supporting Variants
SamplesHGDP00542
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)nssv2561886
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