A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897472



Internal ID22672575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160426572..160426678hg38UCSC Ensembl
chr3:160144360..160144466hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409707
Samples
Known GenesSMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897472
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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