A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3752821



Internal ID12009049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107391212..107391212hg38UCSC Ensembl
chr3:107110059..107110059hg19UCSC Ensembl
chr3:108592749..108592749hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3899
hg1999
hg1899
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1342891
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3752821
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer