A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035034



Internal ID91087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47933776..47961000hg38UCSC Ensembl
chr10:47098903..47126094hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3827225
hg1927192
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422942
Supporting Variants
Samples
Known GenesLINC00842
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035034
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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