A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595072



Internal ID6982391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3907300..4080268hg38UCSC Ensembl
chr3:3948984..4121952hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38172969
hg19172969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10903500, essv10903498, essv10903499, essv10903497, essv10903496
SamplesNA19701, NA19700, NA20798, NA20903, NA07037
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595072
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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