A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560157



Internal ID20933228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179520867..179522761hg38UCSC Ensembl
chr3:179238655..179240549hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381895
hg191895
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5109n223
Supporting Variantsnssv18261150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560157
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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