A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905035



Internal ID22680216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47839849..47839923hg38UCSC Ensembl
chr4:47841866..47841940hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905035
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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