A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561169



Internal ID20934240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160502457..160502914hg38UCSC Ensembl
chr3:160220245..160220702hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260426
Samples
Known GenesKPNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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