A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11049157



Internal ID3940648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77928021..77996385hg38UCSC Ensembl
Innerchr3:77928021..77996385hg38UCSC Ensembl
Outerchr3:77927521..77996885hg38UCSC Ensembl
chr3:77977172..78045536hg19UCSC Ensembl
Innerchr3:77977172..78045536hg19UCSC Ensembl
Outerchr3:77976672..78046036hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3868365
hg1968365
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596675
Supporting Variants
SamplesHG03594
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11049157
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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