A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121179



Internal ID20688219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80790789..80800307hg38UCSC Ensembl
chr4:81711943..81721461hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg389519
hg199519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392486
Supporting Variants
Samples
Known GenesC4orf22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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