A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586909



Internal ID20959980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61986071..61987277hg38UCSC Ensembl
chr16:62019975..62021181hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240022
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586909
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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