A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549477



Internal ID20922638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53278040..53278527hg38UCSC Ensembl
chr3:53312056..53312543hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4877n223
Supporting Variantsnssv18261434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549477
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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