A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035894



Internal ID91673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60396307..60424697hg38UCSC Ensembl
chr10:62156065..62184455hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3828391
hg1928391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484839
Supporting Variants
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035894
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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