A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503035



Internal ID20876285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67480530..67496729hg38UCSC Ensembl
chr16:67514433..67530632hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3816200
hg1916200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179383
Samples
Known GenesAGRP, ATP6V0D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503035
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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