A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569006



Internal ID20942077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169309903..169310782hg38UCSC Ensembl
chr4:170231054..170231933hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264380
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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