A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577269



Internal ID16017992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66552538..66556435hg38UCSC Ensembl
Innerchr18:64219775..64223672hg19UCSC Ensembl
Innerchr18:62370755..62374652hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg383898
hg193898
hg183898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886180
Samples
Known GenesCDH19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577269
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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