A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3997830



Internal ID11417357
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1436907
Supporting Variants
SamplesHuRef
Known GenesCHRNA4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3997830
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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