A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009061



Internal ID7059107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13522112..13522112hg38UCSC Ensembl
chr1:13848607..13848607hg19UCSC Ensembl
chr1:13721194..13721194hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38128
hg19128
hg18128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3570627
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009061
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