A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596055



Internal ID20969126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49060481..49061227hg38UCSC Ensembl
chr20:47677018..47677764hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4481n223
Supporting Variantsnssv18252229
Samples
Known GenesCSE1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596055
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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