A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504096



Internal ID20877356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57270550..57281781hg38UCSC Ensembl
chr16:57304462..57315693hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3811232
hg1911232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193849
Samples
Known GenesPLLP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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