A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524224



Internal ID15451517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40950392..40957664hg38UCSC Ensembl
Innerchr18:38530356..38537628hg19UCSC Ensembl
Innerchr18:36784354..36791626hg18UCSC Ensembl
Innerchr18:36784354..36791626hg17UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg387273
hg197273
hg187273
hg177273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700112
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524224
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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