A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263476



Internal ID20830516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108125316..108126754hg38UCSC Ensembl
chr4:109046472..109047910hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381439
hg191439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568766
Supporting Variants
Samples
Known GenesLEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263476
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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