A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598262



Internal ID6638527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154973905..155196218hg38UCSC Ensembl
chr3:154691694..154914007hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38222314
hg19222314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11190160, essv11190159
SamplesNA21088, NA19661
Known GenesMME
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598262
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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