A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598778



Internal ID20971849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37138941..37139754hg38UCSC Ensembl
chr20:35767344..35768157hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254345
Samples
Known GenesMROH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598778
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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