A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749055



Internal ID21391276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82196544..82200703hg38UCSC Ensembl
chr14:82662888..82667047hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg384160
hg194160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432153
Supporting Variants
SamplesNB12
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749055
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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