A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060574



Internal ID19149793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59984977..60002043hg38UCSC Ensembl
Innerchr18:57652209..57669275hg19UCSC Ensembl
Innerchr18:55803189..55820255hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3817067
hg1917067
hg1817067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3367n100
Supporting Variantsnssv3565517
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)nsv1060574
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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