A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875229



Internal ID22650186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151511232..151511303hg38UCSC Ensembl
chr1:151483708..151483779hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875229
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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