A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265251



Internal ID20832291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40358956..40359032hg38UCSC Ensembl
chr4:40360973..40361049hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265251
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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