A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005594



Internal ID20572635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91152401..91153100hg38UCSC Ensembl
chr12:91546178..91546877hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467514
Supporting Variants
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005594
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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