A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1395867



Internal ID12558989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39469254..39469254hg38UCSC Ensembl
chr3:39510745..39510745hg19UCSC Ensembl
chr3:39485749..39485749hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3714348
SamplesHuRef
Known GenesMOBP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1395867
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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