A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566559



Internal ID20939630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149245248..149252567hg38UCSC Ensembl
chr4:150166400..150173719hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg387320
hg197320
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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