A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4213923



Internal ID11496461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10745377..10745377hg38UCSC Ensembl
chr3:10787062..10787062hg19UCSC Ensembl
chr3:10762062..10762062hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3879
hg1979
hg1879
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1388351
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4213923
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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