A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082635



Internal ID21436204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92929294..92929373hg38UCSC Ensembl
chr14:93395639..93395718hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585011
Supporting Variants
SamplesHG00731
Known GenesCHGA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082635
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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