A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109893



Internal ID20676933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125977620..126037668hg38UCSC Ensembl
chr4:126898775..126958823hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3860049
hg1960049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381141
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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