A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537445



Internal ID20910778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25834163..25835053hg38UCSC Ensembl
chr2:26057032..26057922hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257508
Samples
Known GenesASXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537445
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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