A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526434



Internal ID15453727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36298645..36299442hg38UCSC Ensembl
Innerchr11:36320195..36320992hg19UCSC Ensembl
Innerchr11:36276771..36277568hg18UCSC Ensembl
Innerchr11:36276771..36277568hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38798
hg19798
hg18798
hg17798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702737
Samples
Known GenesPRR5L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526434
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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