A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11070300



Internal ID2230941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95601129..95602814hg38UCSC Ensembl
Innerchr3:95601156..95602788hg38UCSC Ensembl
Outerchr3:95601103..95602841hg38UCSC Ensembl
chr3:95319973..95321658hg19UCSC Ensembl
Innerchr3:95320000..95321632hg19UCSC Ensembl
Outerchr3:95319947..95321685hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381686
hg191686
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597048
Supporting Variants
SamplesHG02006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11070300
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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