A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595487



Internal ID21544093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61308774..61309064hg38UCSC Ensembl
chr14:61775492..61775782hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089022
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595487
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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