A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252421



Internal ID20819461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38901278..38902447hg38UCSC Ensembl
chr1:39366950..39368119hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546825
Supporting Variants
Samples
Known GenesRHBDL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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