A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10950282



Internal ID952098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24842541..24886395hg38UCSC Ensembl
Innerchr3:24842558..24886378hg38UCSC Ensembl
Outerchr3:24842524..24886412hg38UCSC Ensembl
chr3:24884032..24927886hg19UCSC Ensembl
Innerchr3:24884049..24927869hg19UCSC Ensembl
Outerchr3:24884015..24927903hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3843855
hg1943855
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595591
Supporting Variants
SamplesHG03709
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10950282
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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