A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584563



Internal ID20957634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65503360..65504663hg38UCSC Ensembl
chr15:65795698..65797001hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2567n223
Supporting Variantsnssv18238895
Samples
Known GenesDPP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584563
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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