A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265262



Internal ID20832302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42261230..42261902hg38UCSC Ensembl
chr4:42263247..42263919hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560830
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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