A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558153



Internal ID20931224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122499621..122500278hg38UCSC Ensembl
chr3:122218468..122219125hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262425
Samples
Known GenesKPNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558153
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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