A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557820



Internal ID20930891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169827502..169828214hg38UCSC Ensembl
chr3:169545290..169546002hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260466
Samples
Known GenesLRRIQ4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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