A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511401



Internal ID20884728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57273088..57344916hg38UCSC Ensembl
chr16:57307000..57378828hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3871829
hg1971829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182318
Samples
Known GenesPLLP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511401
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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