A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730706



Internal ID20506619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176607747..176607803hg38UCSC Ensembl
chr5:176034748..176034804hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286523
Samples
Known GenesGPRIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730706
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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