A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590957



Internal ID21539529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50675746..50676476hg38UCSC Ensembl
chr10:52435506..52436236hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070317
SamplesNA19240
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590957
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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