A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082047



Internal ID21436426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93768991..93769046hg38UCSC Ensembl
chr14:94235337..94235392hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597797
Supporting Variants
SamplesHG00731
Known GenesPRIMA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082047
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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