A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577069



Internal ID16364478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60600610..60649293hg38UCSC Ensembl
Innerchr18:58267843..58316526hg19UCSC Ensembl
Innerchr18:56418823..56467506hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3848684
hg1948684
hg1848684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5961n54
Supporting Variantsnssv884930
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577069
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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