A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583701



Internal ID20956772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87950256..87950732hg38UCSC Ensembl
chr10:89710013..89710489hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235980
Samples
Known GenesPTEN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583701
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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