A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935324



Internal ID22710664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106185522..106875201hg38UCSC Ensembl
chr14:106642184..107283409hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38689680
hg19641226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372017
Samples
Known GenesLINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935324
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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