A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535828



Internal ID20909182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215105977..215107903hg38UCSC Ensembl
chr2:215970700..215972626hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381927
hg191927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258672
Samples
Known GenesABCA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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