A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1436907



Internal ID12253343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63351228..63351228hg38UCSC Ensembl
chr20:61982580..61982580hg19UCSC Ensembl
chr20:61453024..61453024hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3862
hg1962
hg1862
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3997830
SamplesHuRef
Known GenesCHRNA4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1436907
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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