A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586857



Internal ID20959928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77934372..77935017hg38UCSC Ensembl
chr10:79694130..79694775hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586857
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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