A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595792



Internal ID6983110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33078007..33078933hg38UCSC Ensembl
Innerchr3:33078019..33078922hg38UCSC Ensembl
Outerchr3:33077996..33078945hg38UCSC Ensembl
chr3:33119499..33120425hg19UCSC Ensembl
Innerchr3:33119511..33120414hg19UCSC Ensembl
Outerchr3:33119488..33120437hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10979298, essv10979295, essv10979296, essv10979297
SamplesHG03944, HG03644, HG03745, HG03989
Known GenesGLB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595792
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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