A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381374



Internal ID22439244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66403169..66403837hg38UCSC Ensembl
chr16:66437072..66437740hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939540
Supporting Variants
Samples
Known GenesCDH5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381374
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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