A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271653



Internal ID20480871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92872381..92873528hg38UCSC Ensembl
chr14:93338726..93339873hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743070
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271653
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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