A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263218



Internal ID20830258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151428522..151428823hg38UCSC Ensembl
chr3:151146310..151146611hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566130
Supporting Variants
Samples
Known GenesMED12L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00131


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