A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565282



Internal ID20938353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109695475..109696770hg38UCSC Ensembl
chr4:110616631..110617926hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263562
Samples
Known GenesCASP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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