A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595041



Internal ID6635316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2835751..2838103hg38UCSC Ensembl
Innerchr3:2835751..2838103hg38UCSC Ensembl
Outerchr3:2835515..2838328hg38UCSC Ensembl
chr3:2877435..2879787hg19UCSC Ensembl
Innerchr3:2877435..2879787hg19UCSC Ensembl
Outerchr3:2877199..2880012hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg382353
hg192353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10900085, essv10900084
SamplesHG01029, NA18606
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595041
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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