A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595585



Internal ID20968656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93657202..93657901hg38UCSC Ensembl
chr10:95416959..95417658hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222924
Samples
Known GenesPDE6C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595585
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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