A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561828



Internal ID20934899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138390249..138390970hg38UCSC Ensembl
chr4:139311403..139312124hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5472n223
Supporting Variantsnssv18263158
Samples
Known GenesLINC00499
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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