A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596611



Internal ID20969682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34551294..34551585hg38UCSC Ensembl
chr20:33139098..33139389hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252451
Samples
Known GenesMAP1LC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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