A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059821



Internal ID19149040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:64442723..64606186hg38UCSC Ensembl
Innerchr18:62109958..62273421hg19UCSC Ensembl
Innerchr18:60260938..60424401hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38163464
hg19163464
hg18163464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3378n100
Supporting Variantsnssv3565630
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059821
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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