A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263199



Internal ID20830239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150561871..150562276hg38UCSC Ensembl
chr3:150279658..150280063hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573494
Supporting Variants
Samples
Known GenesEIF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263199
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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