A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11097418



Internal ID3353947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109234688..109247670hg38UCSC Ensembl
Innerchr3:109235188..109247170hg38UCSC Ensembl
Outerchr3:109233688..109248670hg38UCSC Ensembl
chr3:108953535..108966517hg19UCSC Ensembl
Innerchr3:108954035..108966017hg19UCSC Ensembl
Outerchr3:108952535..108967517hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3812983
hg1912983
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597344
Supporting Variants
SamplesHG03007
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11097418
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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