A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044030



Internal ID97085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43466757..43466827hg38UCSC Ensembl
chr11:43488307..43488377hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504714
Supporting Variants
Samples
Known GenesTTC17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044030
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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