A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727466



Internal ID151132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12776204..12817500hg38UCSC Ensembl
chr4:49161593..49202953hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3841297
hg1941361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727466
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.109507


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