A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599043



Internal ID6986091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188922437..188924636hg38UCSC Ensembl
Innerchr3:188922485..188924588hg38UCSC Ensembl
Outerchr3:188922389..188924684hg38UCSC Ensembl
chr3:188640226..188642425hg19UCSC Ensembl
Innerchr3:188640274..188642377hg19UCSC Ensembl
Outerchr3:188640178..188642473hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11265048
SamplesHG02702
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599043
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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