A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253879



Internal ID20820919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81860984..81861582hg38UCSC Ensembl
chr1:82326669..82327267hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542180
Supporting Variants
Samples
Known GenesLPHN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00031


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