A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087931



Internal ID21433784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24209057..24209057hg38UCSC Ensembl
chr14:24678263..24678263hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663677
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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