A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544705



Internal ID20917942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37796322..37797595hg38UCSC Ensembl
chr3:37837813..37839086hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260012
Samples
Known GenesITGA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544705
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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