A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558067



Internal ID20931138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73733714..73754584hg38UCSC Ensembl
chr4:74599431..74620301hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3820871
hg1920871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266023
Samples
Known GenesIL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558067
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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