A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499053



Internal ID20872269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81797974..81803792hg38UCSC Ensembl
chr16:81831579..81837397hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385819
hg195819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033328
Samples
Known GenesPLCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499053
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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