A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103015



Internal ID22012248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36528043..36528043hg38UCSC Ensembl
chr21:37900341..37900341hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639091
Samples
Known GenesCLDN14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103015
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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