A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896370



Internal ID22671462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188613968..188619802hg38UCSC Ensembl
chr3:188331756..188337590hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg385835
hg195835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427965
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896370
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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