A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576934



Internal ID16364343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52607456..52631750hg38UCSC Ensembl
Innerchr18:50133826..50158120hg19UCSC Ensembl
Innerchr18:48387824..48412118hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3824295
hg1924295
hg1824295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5937n54
Supporting Variantsnssv883298
Samples
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576934
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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