A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047289



Internal ID99368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77732334..77733273hg38UCSC Ensembl
chr11:77443379..77444318hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497398
Supporting Variants
Samples
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047289
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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