A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522567



Internal ID15449860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8239751..8242978hg38UCSC Ensembl
Innerchr11:8261298..8264525hg19UCSC Ensembl
Innerchr11:8217874..8221101hg18UCSC Ensembl
Innerchr11:8217874..8221101hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383228
hg193228
hg183228
hg173228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705951
Samples
Known GenesLMO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522567
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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