A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604144



Internal ID21552811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83936261..83936319hg38UCSC Ensembl
chr14:84402605..84402663hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089748
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604144
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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