A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570053



Internal ID21518416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26163321..26163646hg38UCSC Ensembl
chr1:26489812..26490137hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064299
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570053
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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