A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555366



Internal ID20928456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186400039..186598257hg38UCSC Ensembl
chr2:187264766..187462984hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38198219
hg19198219
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256906
Samples
Known GenesITGAV, ZC3H15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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