A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574764



Internal ID20947835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4763963..4764293hg38UCSC Ensembl
chr6:4764197..4764527hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272010
Samples
Known GenesCDYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574764
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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