A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562204



Internal ID20935275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:132113284..132255748hg38UCSC Ensembl
chr4:133034439..133176903hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38142465
hg19142465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562204
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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