A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597048



Internal ID6984362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95601129..95602814hg38UCSC Ensembl
Innerchr3:95601156..95602788hg38UCSC Ensembl
Outerchr3:95601103..95602841hg38UCSC Ensembl
chr3:95319973..95321658hg19UCSC Ensembl
Innerchr3:95320000..95321632hg19UCSC Ensembl
Outerchr3:95319947..95321685hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381686
hg191686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11070300
SamplesHG02006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597048
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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