A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504814



Internal ID20878077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56621050..56630256hg38UCSC Ensembl
chr16:56654962..56664168hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg389207
hg199207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194486
Samples
Known GenesMT1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504814
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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