A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539207



Internal ID20912511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32587038..32587931hg38UCSC Ensembl
chr3:32628530..32629423hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539207
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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