A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520502



Internal ID15447795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60600610..60643110hg38UCSC Ensembl
Innerchr18:58267843..58310343hg19UCSC Ensembl
Innerchr18:56418823..56461323hg18UCSC Ensembl
Innerchr18:56418823..56461323hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3842501
hg1942501
hg1842501
hg1742501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686354, nssv686383, nssv687003, nssv705748, nssv671891
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520502
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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