A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547904



Internal ID20921104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223473820..223476547hg38UCSC Ensembl
chr2:224338538..224341265hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg382728
hg192728
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547904
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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