A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740985



Internal ID20516962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88591877..88592047hg38UCSC Ensembl
chr16:88658285..88658455hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281533
Samples
Known GenesZC3H18
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740985
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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