A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565224



Internal ID21513536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165708162..165708211hg38UCSC Ensembl
chr1:165677399..165677448hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061056
SamplesHG03683
Known GenesLOC440700
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565224
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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