A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4017234



Internal ID11397953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133967840..133967940hg38UCSC Ensembl
chr3:133686684..133686784hg19UCSC Ensembl
chr3:135169374..135169474hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38101
hg19101
hg18101
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1546500
Supporting Variants
SamplesHuRef
Known GenesSLCO2A1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4017234
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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