A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449771



Internal ID227998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23412287..23453963hg38UCSC Ensembl
chr4:23413910..23455586hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3841677
hg1941677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946328
Samples
Known GenesMIR548AJ2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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