A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515764



Internal ID15442821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59984068..60008626hg38UCSC Ensembl
Innerchr18:57651300..57675858hg19UCSC Ensembl
Innerchr18:55802280..55826838hg18UCSC Ensembl
Innerchr18:55802280..55826838hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3824559
hg1924559
hg1824559
hg1724559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658014, nssv669300, nssv668203, nssv664707, nssv679079, nssv684994, nssv689755, nssv656332, nssv674903, nssv684226, nssv690477, nssv693165, nssv687325, nssv684644
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515764
Frequency
Sample Size2026
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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