A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094736



Internal ID20661776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160074273..160076520hg38UCSC Ensembl
chr3:159792060..159794307hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg382248
hg192248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369431
Supporting Variants
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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