A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567545



Internal ID20940616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95357291..95357772hg38UCSC Ensembl
chr4:96278442..96278923hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265446
Samples
Known GenesUNC5C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567545
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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