A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265336



Internal ID20832376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79933756..79934529hg38UCSC Ensembl
chr4:80854910..80855683hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560326
Supporting Variants
Samples
Known GenesANTXR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265336
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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