A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961976



Internal ID22736915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44062596..44062661hg38UCSC Ensembl
chr21:45482477..45482542hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393867
Samples
Known GenesTRAPPC10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961976
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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