A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518823



Internal ID15446116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11361795..11366308hg38UCSC Ensembl
Innerchr11:11383342..11387855hg19UCSC Ensembl
Innerchr11:11339918..11344431hg18UCSC Ensembl
Innerchr11:11339918..11344431hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384514
hg194514
hg184514
hg174514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696275
Samples
Known GenesGALNT18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518823
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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