A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11066215



Internal ID1547940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87926366..87954905hg38UCSC Ensembl
Innerchr3:87926366..87954905hg38UCSC Ensembl
Outerchr3:87925866..87955405hg38UCSC Ensembl
chr3:87975516..88004055hg19UCSC Ensembl
Innerchr3:87975516..88004055hg19UCSC Ensembl
Outerchr3:87975016..88004555hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3828540
hg1928540
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596909
Supporting Variants
SamplesHG01432
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11066215
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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