A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11190085



Internal ID3631949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153995055..154002723hg38UCSC Ensembl
Innerchr3:153995096..154002682hg38UCSC Ensembl
Outerchr3:153995014..154002764hg38UCSC Ensembl
chr3:153712844..153720512hg19UCSC Ensembl
Innerchr3:153712885..153720471hg19UCSC Ensembl
Outerchr3:153712803..153720553hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg387669
hg197669
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598244
Supporting Variants
SamplesHG03229
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11190085
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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