A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544216



Internal ID20917455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47906416..47907004hg38UCSC Ensembl
chr3:47947906..47948494hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4863n223
Supporting Variantsnssv18262102
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544216
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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