A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596346



Internal ID20969417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58961470..58962353hg38UCSC Ensembl
chr20:57536525..57537408hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4502n223
Supporting Variantsnssv18253437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596346
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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