A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031542



Internal ID88732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35282347..35326893hg38UCSC Ensembl
chr10:35571275..35615821hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3844547
hg1944547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493810
Supporting Variants
Samples
Known GenesCCNY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031542
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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