A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543809



Internal ID20917050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152047623..152049212hg38UCSC Ensembl
chr2:152904137..152905726hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg381590
hg191590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254596
Samples
Known GenesCACNB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543809
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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