A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549564



Internal ID20922725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71833593..71834189hg38UCSC Ensembl
chr3:71882744..71883340hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549564
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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