A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120211



Internal ID20687251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75557586..75559740hg38UCSC Ensembl
chr4:76482796..76484950hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg382155
hg192155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393862
Supporting Variants
Samples
Known GenesC4orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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