A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391068



Internal ID22448938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46220747..46220911hg38UCSC Ensembl
chr21:47640661..47640825hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955378
Supporting Variants
Samples
Known GenesLSS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391068
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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