A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890564



Internal ID929248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89062417..89071365hg38UCSC Ensembl
Innerchr10:89062469..89071314hg38UCSC Ensembl
Outerchr10:89062366..89071417hg38UCSC Ensembl
chr10:90822174..90831122hg19UCSC Ensembl
Innerchr10:90822226..90831071hg19UCSC Ensembl
Outerchr10:90822123..90831174hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg388949
hg198949
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624150
Supporting Variants
SamplesHG00554
Known GenesMIR4679-1, MIR4679-2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890564
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