A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598246



Internal ID6985382
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11190091, essv11190090, essv11190095, essv11190096, essv11190087, essv11190093, essv11190094, essv11190092, essv11190089, essv11190088
SamplesNA18917, HG03485, NA19131, HG03575, HG03388, HG02256, HG03557, HG03097, HG03258, HG03351
Known GenesARHGEF26-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598246
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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