A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10987419



Internal ID3524688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38816484..38821828hg38UCSC Ensembl
Innerchr3:38816484..38821828hg38UCSC Ensembl
Outerchr3:38816386..38821936hg38UCSC Ensembl
chr3:38857975..38863319hg19UCSC Ensembl
Innerchr3:38857975..38863319hg19UCSC Ensembl
Outerchr3:38857877..38863427hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg385345
hg195345
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595915
Supporting Variants
SamplesHG03120
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10987419
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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