A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555667



Internal ID20928738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181939203..181939459hg38UCSC Ensembl
chr3:181656991..181657247hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5114n223
Supporting Variantsnssv18261818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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