A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727401



Internal ID151067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11681500..11717288hg38UCSC Ensembl
chr21:9679529..9714516hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3835789
hg1934988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146344
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727401
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.30243


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