A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265929



Internal ID20832969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69616175..69640183hg38UCSC Ensembl
chr4:70481893..70505901hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3824009
hg1924009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565127
Supporting Variants
Samples
Known GenesUGT2A1, UGT2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265929
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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