A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526765



Internal ID20900126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51088780..51105059hg38UCSC Ensembl
chr17:49166141..49182420hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3816280
hg1916280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197003
Samples
Known GenesSPAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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