A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13710258



Internal ID5965468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18771890..18980142hg38UCSC Ensembl
Innerchr10:18771892..18980140hg38UCSC Ensembl
Outerchr10:18771888..18980144hg38UCSC Ensembl
chr10:19060819..19269071hg19UCSC Ensembl
Innerchr10:19060821..19269069hg19UCSC Ensembl
Outerchr10:19060817..19269073hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38208253
hg19208253
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622518
Supporting Variants
SamplesNA19378
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13710258
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