A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571378



Internal ID20944449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124734097..124734765hg38UCSC Ensembl
chr4:125655252..125655920hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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