A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576559



Internal ID16363968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15390016..15408106hg38UCSC Ensembl
Innerchr18:15390015..15408105hg19UCSC Ensembl
Innerchr18:15380015..15398105hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3818091
hg1918091
hg1818091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5871n54
Supporting Variantsnssv878484
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576559
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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