A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956763



Internal ID22731919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9114905..9114984hg38UCSC Ensembl
chr21:9953738..9953817hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402675
Samples
Known GenesTEKT4P2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956763
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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