A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563763



Internal ID20936834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38155324..38155778hg38UCSC Ensembl
chr8:38012842..38013296hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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