A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586274



Internal ID20959345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82253820..82254771hg38UCSC Ensembl
chr15:82546161..82547112hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38952
hg19952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n223
Supporting Variantsnssv18240406
Samples
Known GenesEFTUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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