A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542713



Internal ID20915971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27516489..27516956hg38UCSC Ensembl
chr3:27557980..27558447hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262651
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542713
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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