A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740567



Internal ID20516543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84650387..84653744hg38UCSC Ensembl
chr3:84699538..84702895hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg383358
hg193358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272947
Samples
Known GenesLINC00971
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740567
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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