A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521857



Internal ID8416132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114234873..114258335hg38UCSC Ensembl
Innerchr11:114105595..114129057hg19UCSC Ensembl
Innerchr11:113610805..113634267hg18UCSC Ensembl
Innerchr11:113610805..113634267hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3823463
hg1923463
hg1823463
hg1723463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694631
Samples
Known GenesZBTB16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521857
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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