A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562980



Internal ID20936051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124571863..124572325hg38UCSC Ensembl
chr3:124290710..124291172hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259510
Samples
Known GenesKALRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562980
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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