A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584220



Internal ID20957291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29995585..29996184hg38UCSC Ensembl
chr13:30569722..30570321hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584220
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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