A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261527



Internal ID20828567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57558577..57558954hg38UCSC Ensembl
chr3:57544304..57544681hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546187
Supporting Variants
Samples
Known GenesPDE12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261527
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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