A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400428



Internal ID22458298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36534256..36534370hg38UCSC Ensembl
chr21:37906554..37906668hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952774
Supporting Variants
Samples
Known GenesCLDN14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400428
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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