A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935579



Internal ID2505997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111159140..111241788hg38UCSC Ensembl
chr10:112918898..113001546hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3882649
hg1982649
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624550
Supporting Variants
SamplesHG02224
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935579
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