A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550689



Internal ID20923829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187826584..187862428hg38UCSC Ensembl
chr2:188691311..188727155hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3835845
hg1935845
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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