A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538702



Internal ID20912016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37202648..37204386hg38UCSC Ensembl
chr2:37429791..37431529hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381739
hg191739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260184
Samples
Known GenesCEBPZ, CEBPZ-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538702
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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