A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572084



Internal ID20945155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75937146..75937718hg38UCSC Ensembl
chr4:76858299..76858871hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264691
Samples
Known GenesNAAA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572084
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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