A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595076



Internal ID6635351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3958327..4035443hg38UCSC Ensembl
Innerchr3:3958327..4035443hg38UCSC Ensembl
Outerchr3:3957827..4035943hg38UCSC Ensembl
chr3:4000011..4077127hg19UCSC Ensembl
Innerchr3:4000011..4077127hg19UCSC Ensembl
Outerchr3:3999511..4077627hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3877117
hg1977117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10903520, essv10903522, essv10903521
SamplesNA19701, NA20798, NA20903
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595076
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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