A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892245



Internal ID22667292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155916085..155916178hg38UCSC Ensembl
chr4:156837237..156837330hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416655
Samples
Known GenesTDO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892245
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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