A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520200



Internal ID15447493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43977597..44007585hg38UCSC Ensembl
Innerchr18:41557562..41587550hg19UCSC Ensembl
Innerchr18:39811560..39841548hg18UCSC Ensembl
Innerchr18:39811560..39841548hg17UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3829989
hg1929989
hg1829989
hg1729989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684643, nssv663074, nssv661678
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520200
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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