A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522915



Internal ID299169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81369621..81867737hg38UCSC Ensembl
chr16:81403226..81901342hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38498117
hg19498117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709841
Samples
Known GenesCMIP, GAN, LOC100129617, MIR4720, MIR6504, MIR7854, PLCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522915
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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