A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251023



Internal ID20818063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35811424..35811825hg38UCSC Ensembl
chr1:36277025..36277426hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545467
Supporting Variants
Samples
Known GenesAGO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251023
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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