A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572327



Internal ID20945398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25436764..25437511hg38UCSC Ensembl
chr4:25438386..25439133hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5207n223
Supporting Variantsnssv18265640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572327
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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