A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038832



Internal ID93637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122863033..122904137hg38UCSC Ensembl
chr10:124622549..124663653hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3841105
hg1941105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500267
Supporting Variants
Samples
Known GenesFAM24B, FAM24B-CUZD1, LOC399815
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038832
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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