A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597484



Internal ID6984625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116117205..116164908hg38UCSC Ensembl
Innerchr3:116117205..116164908hg38UCSC Ensembl
Outerchr3:116116705..116165408hg38UCSC Ensembl
chr3:115836052..115883755hg19UCSC Ensembl
Innerchr3:115836052..115883755hg19UCSC Ensembl
Outerchr3:115835552..115884255hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3847704
hg1947704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11111206
SamplesHG01953
Known GenesLSAMP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597484
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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