A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465001



Internal ID22522889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38459438..38467840hg38UCSC Ensembl
chr14:38928642..38937044hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg388403
hg198403
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852009
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465001
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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