A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902135



Internal ID3903951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94900820..94910519hg38UCSC Ensembl
chr10:96660577..96670276hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624263
Supporting Variants
SamplesHG03809
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902135
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