A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893673



Internal ID22668737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188697848..188697923hg38UCSC Ensembl
chr3:188415636..188415711hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428749
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893673
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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