A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648024



Internal ID21840071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11027506..11027616hg38UCSC Ensembl
chrUn_gl000237:41366..41476hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648024
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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