A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444231



Internal ID222611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28807673..28822751hg38UCSC Ensembl
chr4:28809295..28824373hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3815079
hg1915079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947099
Samples
Known GenesMIR4275
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444231
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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