A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596429



Internal ID21545038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4211497..4211667hg38UCSC Ensembl
chr16:4261498..4261668hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088778
SamplesHG03486
Known GenesSRL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596429
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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