A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284324



Internal ID20493542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94363765..94378757hg38UCSC Ensembl
chr14:94830102..94845094hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3814993
hg1914993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731317
Supporting Variants
Samples
Known GenesSERPINA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284324
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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