A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595031



Internal ID6635306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2462723..2486542hg38UCSC Ensembl
chr3:2504407..2528226hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3823820
hg1923820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10899613, essv10899612
SamplesHG04211, NA12058
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595031
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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