A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18055725



Internal ID20622765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190889653..191053150hg38UCSC Ensembl
chr1:190858783..191022280hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38163498
hg19163498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18055725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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