A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570293



Internal ID20943364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120071766..120080354hg38UCSC Ensembl
chr4:120992921..121001509hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg388589
hg198589
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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