A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544863



Internal ID20918101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1289956..1880307hg38UCSC Ensembl
chr3:1331640..1921991hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38590352
hg19590352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259605
Samples
Known GenesCNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544863
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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