A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260287



Internal ID20827327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134171972..134175408hg38UCSC Ensembl
chr3:133890816..133894252hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383437
hg193437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557426
Supporting Variants
Samples
Known GenesRYK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260287
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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