A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903952



Internal ID22679125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172554429..172556273hg38UCSC Ensembl
chr3:172272219..172274063hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381845
hg191845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903952
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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