A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10901978



Internal ID903794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3011255..3026787hg38UCSC Ensembl
chr3:3052939..3068471hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3815533
hg1915533
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595049
Supporting Variants
SamplesNA19031
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10901978
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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