A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13715209



Internal ID3920770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21327903..21338106hg38UCSC Ensembl
chr10:21616832..21627035hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3810204
hg1910204
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622577
Supporting Variants
SamplesHG03572
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13715209
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