A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606766



Internal ID21798813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103291869..103292316hg38UCSC Ensembl
chr14:103758206..103758653hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606766
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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