A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11066175



Internal ID3970396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87854332..87902304hg38UCSC Ensembl
Innerchr3:87854332..87902304hg38UCSC Ensembl
Outerchr3:87853832..87902804hg38UCSC Ensembl
chr3:87903482..87951454hg19UCSC Ensembl
Innerchr3:87903482..87951454hg19UCSC Ensembl
Outerchr3:87902982..87951954hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3847973
hg1947973
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596903
Supporting Variants
SamplesHG03624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11066175
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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