A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597079



Internal ID6984393
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11074024, essv11074028, essv11074026, essv11074027, essv11074029, essv11074030, essv11074025
SamplesHG01840, HG03785, HG02775, HG04017, HG02725, HG03991, HG04153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597079
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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