A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564695



Internal ID21513001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170150057..170150136hg38UCSC Ensembl
chr5:169577061..169577140hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131404
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564695
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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