A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250089



Internal ID20817129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23981269..23982451hg38UCSC Ensembl
chr1:24307759..24308941hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381183
hg191183
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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