A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571338



Internal ID20944409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141935686..141936916hg38UCSC Ensembl
chr3:141654528..141655758hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571338
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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