A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271728



Internal ID20480946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101229938..101230063hg38UCSC Ensembl
chr14:101696275..101696400hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271728
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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