A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577062



Internal ID20950133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99943135..99943778hg38UCSC Ensembl
chr13:100595389..100596032hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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