A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094741



Internal ID20661781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160100301..160101000hg38UCSC Ensembl
chr3:159818088..159818787hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372076
Supporting Variants
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08427


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