A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581328



Internal ID20954399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82286697..82287322hg38UCSC Ensembl
chr13:82860832..82861457hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581328
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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