A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177314



Internal ID20744354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47933901..47988400hg38UCSC Ensembl
chr10:47099028..47151684hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3854500
hg1952657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454795
Supporting Variants
Samples
Known GenesHNRNPA1P33, LINC00842
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01991


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