A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11070351



Internal ID3820054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95628209..95629935hg38UCSC Ensembl
Innerchr3:95628236..95629908hg38UCSC Ensembl
Outerchr3:95628182..95629962hg38UCSC Ensembl
chr3:95347053..95348779hg19UCSC Ensembl
Innerchr3:95347080..95348752hg19UCSC Ensembl
Outerchr3:95347026..95348806hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381727
hg191727
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597050
Supporting Variants
SamplesHG03460
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11070351
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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