A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579195



Internal ID20952266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66669728..66670180hg38UCSC Ensembl
chr16:66703631..66704083hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243577
Samples
Known GenesCMTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579195
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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