A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565084



Internal ID20938155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:51855378..51855811hg38UCSC Ensembl
chr8:52767938..52768371hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278186
Samples
Known GenesPCMTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565084
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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