A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594760



Internal ID20967831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12039623..12040265hg38UCSC Ensembl
chr10:12081622..12082264hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218879
Samples
Known GenesUPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594760
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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