A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10897464



Internal ID899280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:210588..261922hg38UCSC Ensembl
chr3:252271..303605hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3851335
hg1951335
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3594891
Supporting Variants
SamplesNA19780
Known GenesCHL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10897464
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer