A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957124



Internal ID22732264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31379219..31407884hg38UCSC Ensembl
chr21:32751533..32780197hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3828666
hg1928665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404707
Samples
Known GenesTIAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957124
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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