A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567371



Internal ID20940442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152858026..152859115hg38UCSC Ensembl
chr4:153779178..153780267hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381090
hg191090
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263871
Samples
Known GenesARFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567371
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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