A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535424



Internal ID20908785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64457663..64460701hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535424
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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