A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579599



Internal ID20952670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82253934..82254850hg38UCSC Ensembl
chr15:82546275..82547191hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n223
Supporting Variantsnssv18240407
Samples
Known GenesEFTUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579599
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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