A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615578



Internal ID21807625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65386482..65386834hg38UCSC Ensembl
chr14:65853200..65853552hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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