A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572523



Internal ID20945594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170277823..170278308hg38UCSC Ensembl
chr4:171198974..171199459hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572523
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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