A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596142



Internal ID20969213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49773402..49774224hg38UCSC Ensembl
chr20:48389939..48390761hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596142
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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