A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595049



Internal ID6635324
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv862e214
Supporting Variantsessv10901978, essv10901977, essv10901979, essv10901976
SamplesHG01412, NA19448, HG01072, NA19031
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595049
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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