A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13855088



Internal ID2738003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69443738..69453601hg38UCSC Ensembl
chr10:71203494..71213357hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg389864
hg199864
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623745
Supporting Variants
SamplesHG02407
Known GenesTSPAN15
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13855088
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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