A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578242



Internal ID20951313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72465818..72468776hg38UCSC Ensembl
chr13:73039956..73042914hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg382959
hg192959
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578242
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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