A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534481



Internal ID20907842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65760200..65769866hg38UCSC Ensembl
chr17:63756318..63765984hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg389667
hg199667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037861
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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