A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518499



Internal ID15445792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36445264..36458239hg38UCSC Ensembl
Innerchr11:36466814..36479789hg19UCSC Ensembl
Innerchr11:36423390..36436365hg18UCSC Ensembl
Innerchr11:36423390..36436365hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3812976
hg1912976
hg1812976
hg1712976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694243
Samples
Known GenesPRR5L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518499
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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