A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469808



Internal ID22527698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94381524..94404465hg38UCSC Ensembl
chr14:94847861..94870802hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3822942
hg1922942
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861851
Supporting Variants
Samples
Known GenesSERPINA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469808
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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