A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576557



Internal ID16363966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15384564..15409644hg38UCSC Ensembl
Innerchr18:15384563..15409643hg19UCSC Ensembl
Innerchr18:15374563..15399643hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3825081
hg1925081
hg1825081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5870n54
Supporting Variantsnssv878482
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576557
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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