A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565741



Internal ID20938812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86412082..86645441hg38UCSC Ensembl
chr8:87424311..87657669hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38233360
hg19233359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278936
Samples
Known GenesCNGB3, CPNE3, RMDN1, WWP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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