A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029135



Internal ID87121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11283886..11283955hg38UCSC Ensembl
chr10:11325849..11325918hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141883
Supporting Variants
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029135
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005309


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