A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11190097



Internal ID2886442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154034789..154036121hg38UCSC Ensembl
Innerchr3:154034814..154036096hg38UCSC Ensembl
Outerchr3:154034764..154036146hg38UCSC Ensembl
chr3:153752578..153753910hg19UCSC Ensembl
Innerchr3:153752603..153753885hg19UCSC Ensembl
Outerchr3:153752553..153753935hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381333
hg191333
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598247
Supporting Variants
SamplesHG02558
Known GenesARHGEF26-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11190097
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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