A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519371



Internal ID15446664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11280317..11284984hg38UCSC Ensembl
Innerchr11:11301864..11306531hg19UCSC Ensembl
Innerchr11:11258440..11263107hg18UCSC Ensembl
Innerchr11:11258440..11263107hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384668
hg194668
hg184668
hg174668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659008, nssv655728, nssv676956, nssv681368, nssv687392
Samples
Known GenesGALNT18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519371
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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