A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588907



Internal ID20961978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32543279..32543648hg38UCSC Ensembl
chr13:33117416..33117785hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217707
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588907
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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