A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393862



Internal ID21051415
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 StatusM
Merged Variants
Supporting Variantsnssv18120211
Samples
Known GenesC4orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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