A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569792



Internal ID20942863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83941669..83944927hg38UCSC Ensembl
chr4:84862822..84866080hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg383259
hg193259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569792
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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