A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609503



Internal ID21801550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88423674..88423831hg38UCSC Ensembl
chr14:88890018..88890175hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032070
Supporting Variants
Samples
Known GenesSPATA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609503
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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