A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060018



Internal ID21969252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36534256..36534371hg38UCSC Ensembl
chr21:37906554..37906669hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644478
Samples
Known GenesCLDN14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060018
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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