A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252758



Internal ID20819798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93326156..93326851hg38UCSC Ensembl
chr1:93791713..93792408hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548548
Supporting Variants
Samples
Known GenesLOC100131564
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252758
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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