A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565807



Internal ID20938878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119509089..119509694hg38UCSC Ensembl
chr3:119227936..119228541hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4994n223
Supporting Variantsnssv18261746
Samples
Known GenesTIMMDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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