A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734422



Internal ID20510357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32497140..32497620hg38UCSC Ensembl
chr3:32538632..32539112hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267065
Samples
Known GenesCMTM6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734422
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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