A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506461



Internal ID20879741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12677535..12702834hg38UCSC Ensembl
chr16:12771392..12796691hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3825300
hg1925300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197075
Samples
Known GenesCPPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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