A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3882566



Internal ID11879305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17883115..17883115hg38UCSC Ensembl
chr8:17740624..17740624hg19UCSC Ensembl
chr8:17784904..17784904hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3877
hg1977
hg1877
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1012336
Supporting Variants
SamplesHuRef
Known GenesFGL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3882566
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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