A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097997



Internal ID21500277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71765788..71765839hg38UCSC Ensembl
chr14:72232505..72232556hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601830
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097997
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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