A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107936



Internal ID20674976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:130522839..130580983hg38UCSC Ensembl
chr4:131443994..131502138hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3858145
hg1958145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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