A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597020



Internal ID20970091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54644654..54645031hg38UCSC Ensembl
chr20:53261193..53261570hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253362
Samples
Known GenesDOK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597020
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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