A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095341



Internal ID21430982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23925343..23925395hg38UCSC Ensembl
chr14:24394552..24394604hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595735
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095341
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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