A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508959



Internal ID20882264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67266795..67267340hg38UCSC Ensembl
chr16:67300698..67301243hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188622
Samples
Known GenesSLC9A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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