A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892327



Internal ID22667375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165804695..165804801hg38UCSC Ensembl
chr4:166725847..166725953hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427337
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892327
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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