A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3566668



Internal ID7038050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18993945..18993945hg38UCSC Ensembl
chr3:19035437..19035437hg19UCSC Ensembl
chr3:19010441..19010441hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38318
hg19318
hg18318
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989672
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3566668
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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