A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262663



Internal ID20829703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45645967..45646597hg38UCSC Ensembl
chr3:45687459..45688089hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552525
Supporting Variants
Samples
Known GenesLIMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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