A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563471



Internal ID20936542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65715380..65715997hg38UCSC Ensembl
chr8:66627615..66628232hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278470
Samples
Known GenesPDE7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563471
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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