A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573784



Internal ID20946855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180592815..180593525hg38UCSC Ensembl
chr3:180310603..180311313hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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