A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876922



Internal ID22651884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153583091..153583142hg38UCSC Ensembl
chr1:153555567..153555618hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876922
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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