A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893499



Internal ID22668560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23222018..23222144hg38UCSC Ensembl
chr4:23223641..23223767hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414861
Samples
Known GenesMIR548AJ2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893499
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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