A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550106



Internal ID20923258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9454374..9455324hg38UCSC Ensembl
chr3:9496058..9497008hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38951
hg19951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4795n223
Supporting Variantsnssv18264092
Samples
Known GenesSETD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550106
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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