A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898982



Internal ID22674107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150105351..150106173hg38UCSC Ensembl
chr4:151026503..151027325hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417123
Samples
Known GenesDCLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898982
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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