A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084275



Internal ID21435428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61755315..61755382hg38UCSC Ensembl
chr14:62222033..62222100hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599337
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084275
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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