A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590005



Internal ID21538573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102398948..102399468hg38UCSC Ensembl
chr14:102865285..102865805hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094345
SamplesNA19650
Known GenesTECPR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590005
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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