A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590244



Internal ID20963315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19417094..19418885hg38UCSC Ensembl
chr16:19428416..19430207hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381792
hg191792
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239180
Samples
Known GenesTMC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590244
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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