A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895464



Internal ID22670547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39553306..39553701hg38UCSC Ensembl
chr4:39554926..39555321hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426012
Samples
Known GenesMIR1273H, SMIM14, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895464
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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