A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586769



Internal ID21535325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49212698..49212749hg38UCSC Ensembl
chr10:50420743..50420794hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070620
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586769
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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