A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573388



Internal ID20946459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41842325..41843274hg38UCSC Ensembl
chr4:41844342..41845291hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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