A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597038



Internal ID6984352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95014586..95074529hg38UCSC Ensembl
Innerchr3:95014590..95074525hg38UCSC Ensembl
Outerchr3:95014582..95074533hg38UCSC Ensembl
chr3:94733430..94793373hg19UCSC Ensembl
Innerchr3:94733434..94793369hg19UCSC Ensembl
Outerchr3:94733426..94793377hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3859944
hg1959944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11070074, essv11070073, essv11070075
SamplesHG03934, HG03916, HG04153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597038
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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