A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557179



Internal ID20930250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137538355..137547544hg38UCSC Ensembl
chr3:137257197..137266386hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg389190
hg199190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557179
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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