A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649645



Internal ID21841692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12698688..12699024hg38UCSC Ensembl
chrUn_gl000235:6958..7294hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649645
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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