A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13850907



Internal ID4872281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68308472..68310892hg38UCSC Ensembl
Innerchr10:68308472..68310892hg38UCSC Ensembl
Outerchr10:68308472..68310892hg38UCSC Ensembl
chr10:70068229..70070649hg19UCSC Ensembl
Innerchr10:70068229..70070649hg19UCSC Ensembl
Outerchr10:70068229..70070649hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623712
Supporting Variants
SamplesNA12341
Known GenesPBLD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13850907
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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