A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031689



Internal ID88840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41693521..41702275hg38UCSC Ensembl
chr10:42537934..42546687hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388755
hg198754
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420432
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031689
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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