A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597294



Internal ID6637564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106876525..106900950hg38UCSC Ensembl
Innerchr3:106876539..106900936hg38UCSC Ensembl
Outerchr3:106876511..106900964hg38UCSC Ensembl
chr3:106595372..106619797hg19UCSC Ensembl
Innerchr3:106595386..106619783hg19UCSC Ensembl
Outerchr3:106595358..106619811hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3824426
hg1924426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11094672
SamplesNA19901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597294
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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