A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595078



Internal ID6635353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4041939..4088910hg38UCSC Ensembl
Innerchr3:4041951..4088899hg38UCSC Ensembl
Outerchr3:4041928..4088922hg38UCSC Ensembl
chr3:4083623..4130594hg19UCSC Ensembl
Innerchr3:4083635..4130583hg19UCSC Ensembl
Outerchr3:4083612..4130606hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3846972
hg1946972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv863e214
Supporting Variantsessv10903529, essv10903530, essv10903531, essv10903527, essv10903528
SamplesNA19701, NA20798, NA20903, HG04054, HG00254
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595078
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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