A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119086



Internal ID21508654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36523759..36523759hg38UCSC Ensembl
chr21:37896057..37896057hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665082
Supporting Variants
SamplesNA20509
Known GenesCLDN14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119086
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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