A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747363



Internal ID21388606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32938477..32939623hg38UCSC Ensembl
chr14:33407683..33408829hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381147
hg191147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432087
Supporting Variants
SamplesNB08
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747363
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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