A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251330



Internal ID20818370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70273894..70274219hg38UCSC Ensembl
chr1:70739577..70739902hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539425
Supporting Variants
Samples
Known GenesANKRD13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251330
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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