A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647812



Internal ID21839859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11478767..11478851hg38UCSC Ensembl
chrUn_gl000230:18487..18571hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056906
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647812
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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