A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586898



Internal ID21535455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74515506..74516414hg38UCSC Ensembl
chr16:74549404..74550312hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094272
SamplesHG02011
Known GenesGLG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586898
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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