A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743997



Internal ID20519991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187304396..187304703hg38UCSC Ensembl
chr4:188225550..188225857hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272527
Samples
Known GenesLOC339975
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743997
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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