A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887242



Internal ID16181198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70499331..70563787hg38UCSC Ensembl
Innerchr18:68166567..68231023hg19UCSC Ensembl
Innerchr18:66317547..66382003hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3864457
hg1964457
hg1864457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577580
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv887242
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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