A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576696



Internal ID21525137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26961176..26961570hg38UCSC Ensembl
chr1:27287667..27288061hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064378
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576696
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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