A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537446



Internal ID20910779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32116607..32116977hg38UCSC Ensembl
chr2:32341676..32342046hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260057
Samples
Known GenesSPAST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537446
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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