A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100659



Internal ID20667699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45550087..45552530hg38UCSC Ensembl
chr3:45591579..45594022hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382444
hg192444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361849
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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