A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11190088



Internal ID3485753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154028754..154030081hg38UCSC Ensembl
Innerchr3:154028754..154030081hg38UCSC Ensembl
Outerchr3:154028549..154030362hg38UCSC Ensembl
chr3:153746543..153747870hg19UCSC Ensembl
Innerchr3:153746543..153747870hg19UCSC Ensembl
Outerchr3:153746338..153748151hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381328
hg191328
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598246
Supporting Variants
SamplesHG03097
Known GenesARHGEF26-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11190088
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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