A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385325



Internal ID22443195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38678818..38980525hg38UCSC Ensembl
chr14:39148022..39449729hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38301708
hg19301708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944070
Supporting Variants
Samples
Known GenesLINC00639
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385325
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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