A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11063757



Internal ID2904238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86385907..86388164hg38UCSC Ensembl
Innerchr3:86385910..86388162hg38UCSC Ensembl
Outerchr3:86385905..86388167hg38UCSC Ensembl
chr3:86435057..86437314hg19UCSC Ensembl
Innerchr3:86435060..86437312hg19UCSC Ensembl
Outerchr3:86435055..86437317hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg382258
hg192258
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596863
Supporting Variants
SamplesHG02573
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11063757
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer