A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565808



Internal ID20938879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170175973..170177617hg38UCSC Ensembl
chr3:169893761..169895405hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381645
hg191645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260487
Samples
Known GenesPHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565808
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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