A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747106



Internal ID21391159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72686583..72687636hg38UCSC Ensembl
chr3:72735734..72736787hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434085
Supporting Variants
SamplesNB12
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747106
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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