A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035860



Internal ID91651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59896836..59896894hg38UCSC Ensembl
chr10:61656594..61656652hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143708
Supporting Variants
Samples
Known GenesCCDC6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035860
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010332


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