A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247832



Internal ID20814872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209058644..209062460hg38UCSC Ensembl
chr1:209231989..209235805hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg383817
hg193817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247832
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00066


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