A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572620



Internal ID21521012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244781440..244781582hg38UCSC Ensembl
chr1:244944742..244944884hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064046
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572620
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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