A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378826



Internal ID21036379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67690157..67691936hg38UCSC Ensembl
chr4:68555875..68557654hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg381780
hg191780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119476
Samples
Known GenesUBA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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