A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1537664



Internal ID12354099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2705509..2705509hg38UCSC Ensembl
chr3:2747193..2747193hg19UCSC Ensembl
chr3:2722193..2722193hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38621
hg19621
hg18621
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4139859
SamplesHuRef
Known GenesCNTN4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1537664
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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