A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572819



Internal ID20945890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148759811..148762084hg38UCSC Ensembl
chr3:148477598..148479871hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382274
hg192274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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