A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599302



Internal ID6986350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197121103..197122363hg38UCSC Ensembl
Innerchr3:197121127..197122340hg38UCSC Ensembl
Outerchr3:197121080..197122387hg38UCSC Ensembl
chr3:196847974..196849234hg19UCSC Ensembl
Innerchr3:196847998..196849211hg19UCSC Ensembl
Outerchr3:196847951..196849258hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11309343, essv11309342
SamplesHG03873, HG03998
Known GenesDLG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599302
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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