A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723119



Internal ID19021400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66701778..66981041hg38UCSC Ensembl
Innerchr18:64369015..64648278hg19UCSC Ensembl
Innerchr18:62519995..62799258hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38279264
hg19279264
hg18279264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059139
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)nssv3723119
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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