A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591857



Internal ID20964928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14222034..14223133hg38UCSC Ensembl
chr16:14315891..14316990hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239928
Samples
Known GenesMKL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591857
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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