A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253878



Internal ID20820918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81860503..81863274hg38UCSC Ensembl
chr1:82326188..82328959hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382772
hg192772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548056
Supporting Variants
Samples
Known GenesLPHN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253878
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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