A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564039



Internal ID20937110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68504753..68508733hg38UCSC Ensembl
chr6:69214645..69218625hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg383981
hg193981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6242n223
Supporting Variantsnssv18273970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564039
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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