A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093196



Internal ID21501187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97221511..97221564hg38UCSC Ensembl
chr14:97687848..97687901hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598866
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093196
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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