A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584637



Internal ID20957708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76233429..76233538hg38UCSC Ensembl
chr13:76807565..76807674hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584637
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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