A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005628



Internal ID20572669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87073588..87203703hg38UCSC Ensembl
chr12:87467365..87597480hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg38130116
hg19130116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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