A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932969



Internal ID22708276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105462573..105462860hg38UCSC Ensembl
chr14:105928910..105929197hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389040
Samples
Known GenesMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932969
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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