A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727365



Internal ID151032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11118987..11160000hg38UCSC Ensembl
chrUn_gl000236:1..41013hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3841014
hg1941013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727365
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001083


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