A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568351



Internal ID20941422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4225579..4383045hg38UCSC Ensembl
chr4:4227306..4384772hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38157467
hg19157467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265260
Samples
Known GenesLYAR, OTOP1, TMEM128, ZBTB49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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