A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528490



Internal ID15455783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31005672..31103476hg38UCSC Ensembl
Innerchr11:31027219..31125023hg19UCSC Ensembl
Innerchr11:30983795..31081599hg18UCSC Ensembl
Innerchr11:30983795..31081599hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3897805
hg1997805
hg1897805
hg1797805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv61n21
Supporting Variantsnssv705095
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528490
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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