A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569398



Internal ID20942469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182870814..182871799hg38UCSC Ensembl
chr3:182588602..182589587hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5115n223
Supporting Variantsnssv18261833
Samples
Known GenesATP11B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569398
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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