A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566572



Internal ID20939643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42092784..42093475hg38UCSC Ensembl
chr4:42094801..42095492hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566572
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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