A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272892



Internal ID20482110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91105398..91106120hg38UCSC Ensembl
chr14:91571742..91572464hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272892
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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