A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593026



Internal ID21541611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36497097..36497192hg38UCSC Ensembl
chr21:37869395..37869490hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118578
SamplesNA19983
Known GenesCLDN14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593026
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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