A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109331



Internal ID20676371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133296473..133366841hg38UCSC Ensembl
chr4:134217628..134287996hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3870369
hg1970369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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