A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565566



Internal ID21513880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15594136..15610778hg38UCSC Ensembl
chr1:15920631..15937273hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3816643
hg1916643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060845
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565566
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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