A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10949570



Internal ID951386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24082800..24093030hg38UCSC Ensembl
Innerchr3:24082800..24093030hg38UCSC Ensembl
Outerchr3:24082300..24093530hg38UCSC Ensembl
chr3:24124291..24134521hg19UCSC Ensembl
Innerchr3:24124291..24134521hg19UCSC Ensembl
Outerchr3:24123791..24135021hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3810231
hg1910231
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595570
Supporting Variants
SamplesHG01936
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10949570
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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