A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2559495



Internal ID17495125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95185277..95185870hg38UCSC Ensembl
Innerchr9:97947559..97948152hg19UCSC Ensembl
Innerchr9:96987380..96987973hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38594
hg19594
hg18594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972425
Supporting Variants
SamplesHGDP00998
Known GenesFANCC
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)nssv2559495
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