A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589492



Internal ID20962563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68745822..68746323hg38UCSC Ensembl
chr16:68779725..68780226hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243660
Samples
Known GenesCDH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589492
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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