A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3581682



Internal ID6706378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222951467..222951467hg38UCSC Ensembl
chr1:223124809..223124809hg19UCSC Ensembl
chr1:221191432..221191432hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3877
hg1977
hg1877
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991453
Supporting Variants
SamplesHuRef
Known GenesDISP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3581682
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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