A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595931



Internal ID6983249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39580241..39587926hg38UCSC Ensembl
Innerchr3:39580260..39587908hg38UCSC Ensembl
Outerchr3:39580223..39587945hg38UCSC Ensembl
chr3:39621732..39629417hg19UCSC Ensembl
Innerchr3:39621751..39629399hg19UCSC Ensembl
Outerchr3:39621714..39629436hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg387686
hg197686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10987864, essv10987863
SamplesNA21141, NA20849
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595931
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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