A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595761



Internal ID20968832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35198077..35198739hg38UCSC Ensembl
chr20:33785880..33786542hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252483
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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