A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13889928



Internal ID2608880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88384750..88525677hg38UCSC Ensembl
chr10:90144507..90285434hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38140928
hg19140928
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624126
Supporting Variants
SamplesHG02309
Known GenesRNLS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13889928
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer