A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726789



Internal ID150455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36516865..36519780hg38UCSC Ensembl
chr21:37889163..37892078hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg382916
hg192916
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561868
Supporting Variants
Samples
Known GenesCLDN14
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726789
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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