A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600527



Internal ID21549168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84762049..84762098hg38UCSC Ensembl
chr14:85228393..85228442hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091987
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600527
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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