A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253885



Internal ID20820925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82113243..82115954hg38UCSC Ensembl
chr1:82578927..82581638hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382712
hg192712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253885
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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