A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534390



Internal ID20907751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80233247..80246723hg38UCSC Ensembl
chr17:78207046..78220522hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3813477
hg1913477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038463
Samples
Known GenesSLC26A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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