A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479574



Internal ID257093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11893544..11893633hg38UCSC Ensembl
chr10:11935543..11935632hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029192
Samples
Known GenesPROSER2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479574
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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