A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567284



Internal ID20940355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139183254..139183677hg38UCSC Ensembl
chr4:140104408..140104831hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567284
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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