A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568472



Internal ID20941543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94768891..94769179hg38UCSC Ensembl
chr8:95781119..95781407hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279125
Samples
Known GenesDPY19L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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