A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535684



Internal ID20909038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2840466..3629671hg38UCSC Ensembl
chr3:2882150..3671355hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38789206
hg19789206
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261304
Samples
Known GenesCNTN4, CRBN, IL5RA, TRNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535684
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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