A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10979498



Internal ID2149700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34186734..34196448hg38UCSC Ensembl
Innerchr3:34186734..34196448hg38UCSC Ensembl
Outerchr3:34186655..34196567hg38UCSC Ensembl
chr3:34228226..34237940hg19UCSC Ensembl
Innerchr3:34228226..34237940hg19UCSC Ensembl
Outerchr3:34228147..34238059hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg389715
hg199715
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595805
Supporting Variants
SamplesHG01947
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10979498
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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