A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723131



Internal ID19021412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67941356..68114725hg38UCSC Ensembl
Innerchr18:65608593..65781962hg19UCSC Ensembl
Innerchr18:63759573..63932942hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38173370
hg19173370
hg18173370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060561
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3723131
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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