A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265372



Internal ID20832412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91251046..91660618hg38UCSC Ensembl
chr4:92172197..92581769hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38409573
hg19409573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560193
Supporting Variants
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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