A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526201



Internal ID15453494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43565610..43575841hg38UCSC Ensembl
Innerchr18:41145575..41155806hg19UCSC Ensembl
Innerchr18:39399573..39409804hg18UCSC Ensembl
Innerchr18:39399573..39409804hg17UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3810232
hg1910232
hg1810232
hg1710232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702464
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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