A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598431



Internal ID20971502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50174307..50174531hg38UCSC Ensembl
chr20:48790844..48791068hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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