A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536689



Internal ID20910034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68989575..68990417hg38UCSC Ensembl
chr3:69038726..69039568hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4903n223
Supporting Variantsnssv18264018
Samples
Known GenesEOGT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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