A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267065



Internal ID20476283
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 StatusS
Merged Variantsnsv4734422
Supporting Variants
Samples
Known GenesCMTM6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267065
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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