A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558841



Internal ID20931912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40800344..40801639hg38UCSC Ensembl
chr4:40802361..40803656hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264602
Samples
Known GenesNSUN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558841
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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