A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3875104



Internal ID11540081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42989614..42989942hg38UCSC Ensembl
chr3:43031106..43031434hg19UCSC Ensembl
chr3:43006110..43006438hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38329
hg19329
hg18329
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1510992
Supporting Variants
SamplesHuRef
Known GenesFAM198A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3875104
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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