A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10943032



Internal ID4320310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19927106..19941601hg38UCSC Ensembl
Innerchr3:19927106..19941601hg38UCSC Ensembl
Outerchr3:19926606..19942101hg38UCSC Ensembl
chr3:19968598..19983093hg19UCSC Ensembl
Innerchr3:19968598..19983093hg19UCSC Ensembl
Outerchr3:19968098..19983593hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3814496
hg1914496
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595469
Supporting Variants
SamplesHG03869
Known GenesEFHB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10943032
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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