A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261487



Internal ID20828527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56625399..56625844hg38UCSC Ensembl
chr3:56659427..56659872hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546498
Supporting Variants
Samples
Known GenesFAM208A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261487
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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