A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961700



Internal ID22736642
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 StatusM
Merged Variants
Supporting Variantsnssv17396066
Samples
Known GenesCLDN14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961700
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer