A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705029



Internal ID15441681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134484618..134593021hg38UCSC Ensembl
Innerchr11:134354512..134462915hg19UCSC Ensembl
Innerchr11:133859722..133968125hg18UCSC Ensembl
Innerchr11:133859722..133968125hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38108404
hg19108404
hg18108404
hg17108404
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705029
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