A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577331



Internal ID16364740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68041780..68310956hg38UCSC Ensembl
Innerchr18:65709017..65978193hg19UCSC Ensembl
Innerchr18:63859997..64129173hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38269177
hg19269177
hg18269177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886403
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577331
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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