A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391427



Internal ID21382457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120795653..120796735hg38UCSC Ensembl
chr4:121716808..121717890hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703211
Samples
Known GenesPRDM5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391427
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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