A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378476



Internal ID21036029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125426101..125427800hg38UCSC Ensembl
chr4:126347256..126348955hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109278
Samples
Known GenesFAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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