A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577758



Internal ID20950829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30432448..30433124hg38UCSC Ensembl
chr13:31006585..31007261hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1790n223
Supporting Variantsnssv18222010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577758
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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