A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734392



Internal ID20510327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97781296..97781348hg38UCSC Ensembl
chr3:97500140..97500192hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260576
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734392
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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