A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932830



Internal ID22708134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86048168..86161665hg38UCSC Ensembl
chr14:86514512..86628009hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38113498
hg19113498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932830
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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