A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372017



Internal ID22597686
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 StatusS
Merged Variantsnsv5935324
Supporting Variants
Samples
Known GenesLINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372017
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.26


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