A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032954



Internal ID89666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32708883..32719931hg38UCSC Ensembl
chr10:32997811..33008859hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3811049
hg1911049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474804
Supporting Variants
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032954
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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