A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565582



Internal ID20938653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120058003..120058350hg38UCSC Ensembl
chr4:120979158..120979505hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565582
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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