A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566246



Internal ID20939317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64872683..64873129hg38UCSC Ensembl
chr4:65738401..65738847hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5300n223
Supporting Variantsnssv18266521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566246
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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