A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265309



Internal ID20832349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77760100..77761034hg38UCSC Ensembl
chr4:78681254..78682188hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565100
Supporting Variants
Samples
Known GenesCNOT6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265309
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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