A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747016



Internal ID21385319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19819258..19819746hg38UCSC Ensembl
chr16:19830580..19831068hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432322
Supporting Variants
SamplesBTQ055
Known GenesIQCK
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747016
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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