A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262150



Internal ID20829190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48455514..48455927hg38UCSC Ensembl
chr3:48496914..48497327hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554483
Supporting Variants
Samples
Known GenesATRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262150
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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