A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558397



Internal ID20931468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:93681924..93726135hg38UCSC Ensembl
chr4:94603075..94647286hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3844212
hg1944212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265409
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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