A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884994



Internal ID15832264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:63311353..63347135hg38UCSC Ensembl
Innerchr18:60978586..61014368hg19UCSC Ensembl
Innerchr18:59129566..59165348hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3835783
hg1935783
hg1835783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577096
Supporting Variants
Samples
Known GenesBCL2, KDSR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv884994
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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