A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11074029



Internal ID4516509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96680884..96687894hg38UCSC Ensembl
Innerchr3:96680886..96687892hg38UCSC Ensembl
Outerchr3:96680882..96687896hg38UCSC Ensembl
chr3:96399728..96406738hg19UCSC Ensembl
Innerchr3:96399730..96406736hg19UCSC Ensembl
Outerchr3:96399726..96406740hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg387011
hg197011
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597079
Supporting Variants
SamplesHG04017
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11074029
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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