A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597863



Internal ID20970934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17550475..17551723hg38UCSC Ensembl
chr20:17531120..17532368hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253586
Samples
Known GenesBFSP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597863
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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