A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682694



Internal ID15072660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45881643..45961834hg38UCSC Ensembl
Innerchr11:45903194..45983385hg19UCSC Ensembl
Innerchr11:45859770..45939961hg18UCSC Ensembl
Innerchr11:45859770..45939961hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3880192
hg1980192
hg1880192
hg1780192
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516442
Supporting Variants
Samples
Known GenesC11orf94, CRY2, GYLTL1B, MAPK8IP1, PEX16, PHF21A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682694
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