A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048646



Internal ID100305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78772636..78772699hg38UCSC Ensembl
chr11:78483681..78483744hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495862
Supporting Variants
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048646
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.011239


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