A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081571



Internal ID21460096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100202751..100202857hg38UCSC Ensembl
chr14:100669088..100669194hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603472
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081571
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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