A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576243



Internal ID16016966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:594262..631435hg38UCSC Ensembl
Innerchr18:594262..631435hg19UCSC Ensembl
Innerchr18:584262..621435hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3837174
hg1937174
hg1837174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877295
Samples
Known GenesCLUL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576243
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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