A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503062



Internal ID20876313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66880904..66904846hg38UCSC Ensembl
chr16:66914807..66938749hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3823943
hg1923943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188847
Samples
Known GenesPDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503062
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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