A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053408



Internal ID103452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124973677..124981145hg38UCSC Ensembl
chr11:124843573..124851041hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg387469
hg197469
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556070
Supporting Variants
Samples
Known GenesCCDC15
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053408
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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