A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400478



Internal ID22458348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41081568..41087592hg38UCSC Ensembl
chr21:42453495..42459519hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg386025
hg196025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400478
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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