A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250450



Internal ID20817490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60776793..60778810hg38UCSC Ensembl
chr1:61242465..61244482hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg382018
hg192018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00071


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