A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13690315



Internal ID3789065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8238490..8248891hg38UCSC Ensembl
Innerchr10:8238490..8248891hg38UCSC Ensembl
Outerchr10:8237990..8249391hg38UCSC Ensembl
chr10:8280453..8290854hg19UCSC Ensembl
Innerchr10:8280453..8290854hg19UCSC Ensembl
Outerchr10:8279953..8291354hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810402
hg1910402
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622284
Supporting Variants
SamplesHG03437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13690315
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