A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876426



Internal ID22651387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221498888..221501376hg38UCSC Ensembl
chr1:221672230..221674718hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382489
hg192489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876426
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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