A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564708



Internal ID21513014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196142168..196142219hg38UCSC Ensembl
chr3:195869039..195869090hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133222
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564708
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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