A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559478



Internal ID20932549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159953616..160766414hg38UCSC Ensembl
chr4:160874768..161687566hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38812799
hg19812799
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559478
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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