A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903884



Internal ID22679056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165039500..165039821hg38UCSC Ensembl
chr4:165960652..165960973hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413803
Samples
Known GenesTRIM60
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903884
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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