A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048920



Internal ID21958154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11027675..11027783hg38UCSC Ensembl
chrUn_gl000237:41199..41307hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048920
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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