A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935464



Internal ID22710806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75054235..75058815hg38UCSC Ensembl
chr14:75520938..75525518hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384581
hg194581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387878
Samples
Known GenesACYP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935464
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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