A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053557



Internal ID103552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132319287..132320281hg38UCSC Ensembl
chr11:132189181..132190175hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494972
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053557
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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