A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13757264



Internal ID4650435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37920950..37922907hg38UCSC Ensembl
Innerchr10:37921000..37922857hg38UCSC Ensembl
Outerchr10:37920828..37923029hg38UCSC Ensembl
chr10:38209878..38211835hg19UCSC Ensembl
Innerchr10:38209928..38211785hg19UCSC Ensembl
Outerchr10:38209756..38211957hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg381958
hg191958
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622974
Supporting Variants
SamplesHG04180
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13757264
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