A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560794



Internal ID20933865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4278312..4292501hg38UCSC Ensembl
chr4:4280039..4294228hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3814190
hg1914190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265663
Samples
Known GenesLYAR, ZBTB49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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