A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570347



Internal ID20943418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170478224..170478909hg38UCSC Ensembl
chr3:170196012..170196697hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260517
Samples
Known GenesSLC7A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570347
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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