A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874188



Internal ID22649139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154657925..154695812hg38UCSC Ensembl
chr1:154630401..154668288hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3837888
hg1937888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874188
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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