A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093871



Internal ID21447809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71167959..71168076hg38UCSC Ensembl
chr14:71634676..71634793hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585788
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093871
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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