A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1396412



Internal ID12212848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2389261..2389322hg38UCSC Ensembl
chr3:2430945..2431006hg19UCSC Ensembl
chr3:2405945..2406006hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3862
hg1962
hg1862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4090083
SamplesHuRef
Known GenesCNTN4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1396412
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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