A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598607



Internal ID20971678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44514729..44515733hg38UCSC Ensembl
chr20:43143370..43144374hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252102
Samples
Known GenesSERINC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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