A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901055



Internal ID22676203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149661983..149671174hg38UCSC Ensembl
chr4:150583135..150592326hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg389192
hg199192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901055
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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