A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885025



Internal ID22660009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40880589..40915351hg38UCSC Ensembl
chr1:41346261..41381023hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3834763
hg1934763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885025
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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