A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576805



Internal ID20949876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18276631..18277074hg38UCSC Ensembl
chr10:18565560..18566003hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220034
Samples
Known GenesCACNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576805
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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