A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726092



Internal ID18677687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:63138366..63181655hg38UCSC Ensembl
Innerchr18:60805599..60848888hg19UCSC Ensembl
Innerchr18:58956579..58999868hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3843290
hg1943290
hg1843290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057080
Supporting Variants
Samples
Known GenesBCL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726092
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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