A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118571



Internal ID21405667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36492138..36492459hg38UCSC Ensembl
chr21:37864436..37864757hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598556
Supporting Variants
SamplesHG00512
Known GenesCLDN14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118571
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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