A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554649



Internal ID20927743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9426672..9427252hg38UCSC Ensembl
chr3:9468356..9468936hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264086
Samples
Known GenesSETD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554649
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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