A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905609



Internal ID22680798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37857442..37857533hg38UCSC Ensembl
chr4:37859063..37859154hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413370
Samples
Known GenesPGM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905609
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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