A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296876



Internal ID20506094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88423671..88423827hg38UCSC Ensembl
chr14:88890015..88890171hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742838
Supporting Variants
Samples
Known GenesSPATA7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296876
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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