A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596277



Internal ID20969348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35716017..35717018hg38UCSC Ensembl
chr20:34303939..34304940hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252504
Samples
Known GenesRBM39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596277
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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