A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567675



Internal ID20940746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98875729..98876195hg38UCSC Ensembl
chr4:99796880..99797346hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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