A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249779



Internal ID20816819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53227642..53228150hg38UCSC Ensembl
chr1:53693314..53693822hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542472
Supporting Variants
Samples
Known GenesMAGOH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249779
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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