A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580665



Internal ID20953736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6496197..6496651hg38UCSC Ensembl
chr10:6538159..6538613hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221639
Samples
Known GenesPRKCQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580665
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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