A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13701454



Internal ID593293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14378913..14379485hg38UCSC Ensembl
Innerchr10:14378913..14379485hg38UCSC Ensembl
Outerchr10:14378641..14379747hg38UCSC Ensembl
chr10:14420912..14421484hg19UCSC Ensembl
Innerchr10:14420912..14421484hg19UCSC Ensembl
Outerchr10:14420640..14421746hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622422
Supporting Variants
SamplesHG00259
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13701454
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