A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895186



Internal ID22670264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104946404..105445672hg38UCSC Ensembl
chr4:105867561..106366829hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38499269
hg19499269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416193
Samples
Known GenesPPA2, TET2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895186
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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