A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573209



Internal ID20946280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142620153..142620825hg38UCSC Ensembl
chr3:142338995..142339667hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262480
Samples
Known GenesPLS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573209
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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