A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595080



Internal ID6635355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4046785..4059743hg38UCSC Ensembl
Innerchr3:4046800..4059729hg38UCSC Ensembl
Outerchr3:4046771..4059758hg38UCSC Ensembl
chr3:4088469..4101427hg19UCSC Ensembl
Innerchr3:4088484..4101413hg19UCSC Ensembl
Outerchr3:4088455..4101442hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3812959
hg1912959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10903543, essv10903536, essv10903537, essv10903541, essv10903539, essv10903538, essv10903542, essv10903540
SamplesNA19701, HG01305, HG01686, NA20798, NA20903, HG04054, HG00254, NA12873
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595080
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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