A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1541174



Internal ID12357609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2746143..2746143hg38UCSC Ensembl
chr3:2787827..2787827hg19UCSC Ensembl
chr3:2762827..2762827hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3859
hg1959
hg1859
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4187758
SamplesHuRef
Known GenesCNTN4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1541174
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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