A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595735



Internal ID21544342
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 StatusM
Merged Variants
Supporting Variantsnssv17095341
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595735
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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