A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005563



Internal ID20572604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90963101..90970100hg38UCSC Ensembl
chr12:91356878..91363877hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467795
Supporting Variants
Samples
Known GenesEPYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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