A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872906



Internal ID22647848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116714220..116730494hg38UCSC Ensembl
chr1:117256842..117273116hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3816275
hg1916275
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358284
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872906
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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