A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035036



Internal ID91089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47944368..47984368hg38UCSC Ensembl
chr10:47109471..47149482hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3840001
hg1940012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144043
Supporting Variants
Samples
Known GenesHNRNPA1P33, LINC00842
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035036
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.047461


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