A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263201



Internal ID20830241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150572855..150573317hg38UCSC Ensembl
chr3:150290642..150291104hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565318
Supporting Variants
Samples
Known GenesEIF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263201
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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