A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559074



Internal ID20932145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3463857..3464737hg38UCSC Ensembl
chr6:3464091..3464971hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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