A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3973296



Internal ID11441890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63353917..63353917hg38UCSC Ensembl
chr20:61985269..61985269hg19UCSC Ensembl
chr20:61455713..61455713hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38120
hg19120
hg18120
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1443132
Supporting Variants
SamplesHuRef
Known GenesCHRNA4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3973296
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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