A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10897462



Internal ID899278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:210588..261922hg38UCSC Ensembl
chr3:252271..303605hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3851335
hg1951335
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3594890
Supporting Variants
SamplesHG02238
Known GenesCHL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10897462
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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