A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564002



Internal ID20937073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119504938..119505661hg38UCSC Ensembl
chr3:119223785..119224508hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261744
Samples
Known GenesTIMMDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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