A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952559



Internal ID22727872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181124517..181124517hg38UCSC Ensembl
chr1:181093653..181093653hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952559
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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