A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093248



Internal ID21470178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20506846..20507022hg38UCSC Ensembl
chr14:20975005..20975181hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595484
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093248
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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