A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537940



Internal ID20911267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68978654..68980772hg38UCSC Ensembl
chr3:69027805..69029923hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264016
Samples
Known GenesEOGT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537940
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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