A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666690



Internal ID15403342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67734155..67947557hg38UCSC Ensembl
Innerchr11:67501626..67715028hg19UCSC Ensembl
Innerchr11:67258202..67471604hg18UCSC Ensembl
Innerchr11:67258202..67471604hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38213403
hg19213403
hg18213403
hg17213403
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516191
Supporting Variants
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666690
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer