A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524019



Internal ID15451312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11272119..11272706hg38UCSC Ensembl
Innerchr11:11293666..11294253hg19UCSC Ensembl
Innerchr11:11250242..11250829hg18UCSC Ensembl
Innerchr11:11250242..11250829hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38588
hg19588
hg18588
hg17588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699880
Samples
Known GenesGALNT18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524019
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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